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- pompeepeepompeepee
  ·2021-09-19
  oof
  FDA Advisory Committee Votes Unanimously in Favor of COMIRNATY® Booster for Emergency Use in People 65 and Older and Certain High-Risk Populations
  Committee reviewed clinical data showing a booster dose of COMIRNATY® elicits high neutralization ti
  FDA Advisory Committee Votes Unanimously in Favor of COMIRNATY® Booster for Emergency Use in People 65 and Older and Certain High-Risk Populations
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- pompeepeepompeepee
  ·2021-08-24
  whee
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- pompeepeepompeepee
  ·2021-08-18
  wa
  3 Stocks Warren Buffett Is Selling That You Should Be Buying Hand Over Fist
  Berkshire Hathaway's stakes in these top-tier companies were reduced during the second quarter.
  3 Stocks Warren Buffett Is Selling That You Should Be Buying Hand Over Fist
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- pompeepeepompeepee
  ·2021-08-11
  wow
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- pompeepeepompeepee
  ·2021-08-09
  likee
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- pompeepeepompeepee
  ·2021-08-08
  yay
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- pompeepeepompeepee
  ·2021-08-06
  yay
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- pompeepeepompeepee
  ·2021-08-03
  wah
  August is among the worst months of year for the stock market. Here's how to play it.
  On Wall Street, August is off to a solid start, but the month tends to accompany a bout of turbulenc
  August is among the worst months of year for the stock market. Here's how to play it.
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- pompeepeepompeepee
  ·2021-08-03
  wah
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- pompeepeepompeepee
  ·2021-08-02
  wowew
  Commodities Week Ahead: Oil, Gold Eye U.S. Jobs Report As China PMI Slides
  It’s that time again. The release of the monthly US jobs report. And the direction of gold, oil and
  Commodities Week Ahead: Oil, Gold Eye U.S. Jobs Report As China PMI Slides
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15:40","market":"us","language":"en","title":"FDA Advisory Committee Votes Unanimously in Favor of COMIRNATY® Booster for Emergency Use in People 65 and Older and Certain High-Risk Populations","url":"https://stock-news.laohu8.com/highlight/detail?id=2168957763","media":"StreetInsider","summary":"Committee reviewed clinical data showing a booster dose of COMIRNATY® elicits high neutralization ti","content":"<ul>\n <li><i>Committee reviewed clinical data showing a booster dose of COMIRNATY® elicits high neutralization titers against SARS-CoV-2 and all currently tested variants </i></li>\n <li><i>Reactogenicity profile within seven days of the booster dose was typically mild to moderate, with frequency of reactions similar to or lower than after the primary vaccination series</i></li>\n <li><i>Real-world data presented by Israel Ministry of Health show additional protection after receiving a</i> <i>booster translated to vaccine effectiveness comparable to levels seen early in the country’s vaccine</i> <i>rollout</i></li>\n <li><i>FDA expected to make its decision in the coming days </i></li>\n</ul>\n<p><b>NEW YORK AND MAINZ, GERMANY, September 17, 2021</b>—Pfizer Inc. (NYSE: PFE) and <a href=\"https://laohu8.com/S/BNTX\">BioNTech SE</a> (Nasdaq: BNTX) announced today that the U.S. Food and Drug Administration’s (FDA) Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted unanimously to recommend the FDA grant Emergency Use Authorization (EUA) for a booster dose of COMIRNATY® (COVID-19 Vaccine, mRNA) in individuals 65 years of age and older and individuals at high risk of severe COVID-19. The committee recommended that the additional dose be administered at least six months after the two-dose series. The panel also agreed that healthcare workers and others at high risk for occupational exposure should be included in this EUA.</p>\n<p>VRBPAC is made up of independent experts who advise the FDA on scientific and regulatory matters, including the evaluation of vaccine safety and efficacy.</p>\n<p>At this time, VRBPAC did not vote in favor of approval of a booster dose for the full population for which Pfizer and BioNTech submitted their supplemental Biologics License Application, which was individuals 16 and older. The same data have recently been submitted to the European Medicines Agency (EMA) and will be filed with other regulatory authorities in the coming weeks. The companies remain vigilant and continue to generate relevant COMIRNATY booster dose data for evaluation for future licensure in further groups as well as to address emerging variants of concern.</p>\n<p>The FDA is expected to make its decision in the coming days. This decision could allow COMIRNATY to be the first COVID-19 vaccine with a booster authorized in the U.S.</p>\n<p>“Today the VRBPAC reviewed data from our clinical program showing a favorable safety profile and strong immune responses against SARS-CoV-2 after a booster dose of our vaccine. These data, and the larger body of scientific evidence presented at the meeting, underscore our belief that boosters can be a critical tool in the ongoing effort to control the spread of this virus,” said <b>Kathrin U. Jansen, Ph.D., Senior Vice President and Head of Vaccine Research &amp; Development, Pfizer</b>. “We thank the committee for their thoughtful review of the data and will work with the FDA following today’s meeting to address the committee’s questions, as we continue to believe in the benefits of a booster dose for a broader population.”</p>\n<p>“We are committed to support the ongoing efforts to reduce infections and COVID-19 cases. The data we submitted to the FDA, EMA and other regulatory authorities underline that a booster induces a strong immune response against all tested variants of concern and may contribute to address a public health need,” said <b>Özlem Türeci, M.D., Co-founder and Chief Medical Officer of BioNTech.</b></p>\n<p>VRBPAC based its recommendation on the totality of scientific evidence shared by the companies, including data from their clinical program evaluating the safety, tolerability and immunogenicity of a booster dose of COMIRNATY. A booster dose of the vaccine elicited significantly higher neutralizing antibody titers against the initial SARS-CoV-2 virus (wild type), as well as the Beta and Delta variants, when compared with the levels observed after the two-dose primary series. The reactogenicity profile within seven days after the booster dose was typically mild to moderate, and the frequency of reactions was similar to or lower than after dose two. The adverse event profile was generally consistent with other clinical safety data for COMIRNATY.</p>\n<p>Real-world surveillance data also were presented to the VRBPAC by the Israel Ministry of Health, providing further support for the public health impact of boosters. The data presented from Israel included an analysis published this week in <i>The New England Journal of Medicine</i>. The analysis comprised approximately 1.1 million individuals ages 60 years and older who were eligible for a booster dose of the vaccine between July 30 through August 31, 2021. No new safety signals were observed, and reported adverse events were lower than those observed after dose two. The analysis showed that a booster dose restored very high levels of protection against COVID-19 infections and severe disease in this period when Delta was the dominant strain. Individuals who received the booster dose were less likely by a factor of 11.3 (95% CI: 10.4, 12.3) to develop a confirmed infection and less likely by a factor of 19.5 (95% CI: 12.9, 29.5) to develop severe illness compared to those who were previously fully vaccinated but did not receive a booster dose. The additional protection after receiving a booster translated to vaccine effectiveness comparable to levels seen early in the country’s vaccine rollout (an estimated 95%), when the Alpha variant was predominant.</p>\n<p>Under the EUA of the Pfizer-BioNTech vaccine in the U.S., a third dose was <u>previously authorized</u> for individuals at least 12 years of age who have undergone solid organ transplant, or who are diagnosed with conditions that are considered to have an equivalent level of immunocompromise. This authorization of a third dose for immunocompromised individuals is separate and distinct from the booster dose reviewed by VRBPAC today. The third dose for immunocompromised individuals is meant to address the fact that these individuals sometimes do not build enough protection after two doses of the vaccine. In contrast, the booster dose recommended today by VRBPAC for EUA refers to an additional dose of the vaccine that is given to those who have built enough protection after the primary two-dose vaccination series, but may have decreased protection over time due to waning of immunity.</p>\n<p>COMIRNATY, which is based on BioNTech’s proprietary mRNA technology, was developed by both BioNTech and Pfizer. BioNTech is the Marketing Authorization Holder in the United States, the European Union, the United Kingdom, Canada and the holder of emergency use authorizations or equivalents in the United States (jointly with Pfizer) and other countries. Submissions to pursue regulatory approvals in those countries where emergency use authorizations or equivalent were initially granted are planned.</p>\n<p><b>U.S. Indication &amp; Authorized Use</b>COMIRNATY® (COVID-19 Vaccine, mRNA) is an FDA-approved COVID-19 vaccine made by Pfizer for BioNTech.</p>\n<ul>\n <li>It is approved as a 2-dose series for prevention of COVID-19 in individuals 16 years of age and older</li>\n <li>It is also authorized under Emergency Use Authorization (EUA) to be administered for emergency use to:</li>\n</ul>\n<p>The Pfizer-BioNTech COVID-19 Vaccine has received EUA from FDA to:</p>\n<ul>\n <li>prevent COVID-19 in individuals 12 years of age and older, and</li>\n <li>provide a third dose to individuals 12 years of age and older who have been determined to have certain kinds of immunocompromise</li>\n</ul>\n<p>The FDA-approved COMIRNATY® (COVID-19 Vaccine, mRNA) and the EUA-authorized Pfizer-BioNTech COVID-19 Vaccine have the same formulation and can be used interchangeably to provide the COVID-19 vaccination series. An individual may be offered either COMIRNATY® (COVID-19 Vaccine, mRNA) or the Pfizer-BioNTech COVID-19 Vaccine to prevent coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2.</p>\n<p><b>EUA Statement</b>This emergency use of the product has not been approved or licensed by FDA, but has been authorized by FDA under an Emergency Use Authorization (EUA) to prevent Coronavirus Disease 2019 (COVID-19) for use in individuals 12 years of age and older; and the emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of the medical product under Section 564(b)(1) of the FD&amp;C Act unless the declaration is terminated or authorization revoked sooner.</p>\n<p><b>Important Safety Information</b>Individuals should <b>not</b> get the Pfizer-BioNTech COVID-19 Vaccine if they:</p>\n<ul>\n <li>had a severe allergic reaction after a previous dose of this vaccine</li>\n <li>had a severe allergic reaction to any ingredient of this vaccine</li>\n</ul>\n<p>Individuals should tell the vaccination provider about all of their medical conditions, including if they:</p>\n<ul>\n <li>have any allergies</li>\n <li>have had myocarditis (inflammation of the heart muscle) or pericarditis (inflammation of the lining outside the heart)</li>\n <li>have a fever</li>\n <li>have a bleeding disorder or are on a blood thinner</li>\n <li>are immunocompromised or are on a medicine that affects the immune system</li>\n <li>are pregnant, plan to become pregnant, or are breastfeeding</li>\n <li>have received another COVID-19 vaccine</li>\n <li>have ever fainted in association with an injection</li>\n</ul>\n<p>The vaccine may not protect everyone.</p>\n<p>Side effects reported with the vaccine include:</p>\n<ul>\n <li>There is a remote chance that the vaccine could cause a severe allergic reaction</li>\n <li>Myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the lining outside the heart) have occurred in some people who have received the vaccine. In most of these people, symptoms began within a few days following receipt of the second dose of the vaccine. The chance of having this occur is very low. Individuals should seek medical attention right away if they have any of the following symptoms after receiving the vaccine:</li>\n <li>Side effects that have been reported with the vaccine include:</li>\n <li>These may not be all the possible side effects of the vaccine. Serious and unexpected side effects may occur. The vaccine is still being studied in clinical trials. Call the vaccination provider or healthcare provider about bothersome side effects or side effects that do not go away</li>\n</ul>\n<p>There is no information on the use of the vaccine with other vaccines.</p>\n<p>Patients should always ask their healthcare providers for medical advice about adverse events. Individuals are encouraged to report negative side effects of vaccines to the US Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC). Visit <u>http://www.vaers.hhs.gov</u> or call 1-800-822-7967. In addition, side effects can be reported to Pfizer Inc. at <u>www.pfizersafetyreporting.com</u> or by calling 1-800-438-1985.</p>\n<p>Please <u>click here</u> for full Prescribing Information (16+ years of age). Please <u>click here</u> for Fact Sheet for Vaccination Providers (12+ years of age).</p>\n<p><b>About Pfizer: Breakthroughs That Change Patients’ Lives</b>At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products, including innovative medicines and vaccines. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as one of the world's premier innovative biopharmaceutical companies, we collaborate with health care providers, governments and local communities to support and expand access to reliable, affordable health care around the world. For more than 170 years, we have worked to make a difference for all who rely on us. We routinely post information that may be important to investors on our website at <u>www.Pfizer.com</u>. In addition, to learn more, please visit us on <u>www.Pfizer.com</u> and follow us on <a href=\"https://laohu8.com/S/TWTR\">Twitter</a> at <u>@Pfizer</u> and <u>@Pfizer News</u>, <u>LinkedIn</u>, <u>YouTube</u> and like us on <a href=\"https://laohu8.com/S/FB\">Facebook</a> at <u>Facebook.com/Pfizer</u>.</p>\n<p><b>Pfizer Disclosure Notice</b>The information contained in this release is as of September 17, 2021. Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments.</p>\n<p>This release contains forward-looking information about Pfizer’s efforts to combat COVID-19, the collaboration between BioNTech and Pfizer to develop a COVID-19 vaccine, the BNT162 mRNA vaccine program and COMIRNATY (COVID-19 Vaccine, mRNA) (BNT162b2) (including a potential booster (third) dose and a supplemental Biologics License Application (sBLA) for a potential booster (third) dose of BNT162b2 in individuals 16 years of age and older in the U.S., qualitative assessments of available data, potential benefits, expectations for clinical trials, the anticipated timing of regulatory submissions, regulatory approvals or authorizations and anticipated manufacturing, distribution and supply) involving substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. Risks and uncertainties include, among other things, the uncertainties inherent in research and development, including the ability to meet anticipated clinical endpoints, commencement and/or completion dates for clinical trials, regulatory submission dates, regulatory approval dates and/or launch dates, as well as risks associated with preclinical and clinical data (including the Phase 3 data), including the possibility of unfavorable new preclinical, clinical or safety data and further analyses of existing preclinical, clinical or safety data; whether and when our Phase 3 clinical trial will demonstrate protection from infection or disease following a booster (third) dose, which is the subject of ongoing study; the ability to produce comparable clinical or other results, including the rate of vaccine effectiveness and safety and tolerability profile observed to date, in additional analyses of the Phase 3 trial and additional studies or in larger, more diverse populations following commercialization; the ability of BNT162b2 to prevent COVID-19 caused by emerging virus variants; the risk that more widespread use of the vaccine will lead to new information about efficacy, safety, or other developments, including the risk of additional adverse reactions, some of which may be serious; the risk that preclinical and clinical trial data are subject to differing interpretations and assessments, including during the peer review/publication process, in the scientific community generally, and by regulatory authorities; whether and when additional data from the BNT162 mRNA vaccine program will be published in scientific journal publications and, if so, when and with what modifications and interpretations; whether regulatory authorities will be satisfied with the design of and results from these and any future preclinical and clinical studies; whether and when applications for a potential booster (third) dose will be filed in any other jurisdictions and whether and when other biologics license and/or emergency use authorization applications or amendments to any such applications may be filed in particular jurisdictions for BNT162b2 or any other potential vaccines that may arise from the BNT162 program, and if obtained, whether or when such emergency use authorization or licenses will expire or terminate; whether and when any applications that may be pending or filed for BNT162b2 (including the sBLA for a potential booster (third) dose in the U.S., applications that may be pending or filed for a potential booster (third) dose in other jurisdictions or any requested amendments to the emergency use or conditional marketing authorizations) or other vaccines that may result from the BNT162 program may be approved by particular regulatory authorities, which will depend on myriad factors, including making a determination as to whether the vaccine’s benefits outweigh its known risks and determination of the vaccine’s efficacy and, if approved, whether it will be commercially successful; decisions by regulatory authorities impacting labeling or marketing, manufacturing processes, safety and/or other matters that could affect the availability or commercial potential of a vaccine, including development of products or therapies by other companies; disruptions in the relationships between us and our collaboration partners, clinical trial sites or third-party suppliers; the risk that demand for any products may be reduced or no longer exist; risks related to the availability of raw materials to manufacture a vaccine; challenges related to our vaccine’s ultra-low temperature formulation, two-dose schedule and attendant storage, distribution and administration requirements, including risks related to storage and handling after delivery by Pfizer; the risk that we may not be able to successfully develop other vaccine formulations, booster doses or new variant-specific vaccines; the risk that we may not be able to create or scale up manufacturing capacity on a timely basis or maintain access to logistics or supply channels commensurate with global demand for our vaccine, which would negatively impact our ability to supply the estimated numbers of doses of our vaccine within the projected time periods as previously indicated; whether and when additional supply agreements will be reached; uncertainties regarding the ability to obtain recommendations from vaccine advisory or technical committees and other public health authorities and uncertainties regarding the commercial impact of any such recommendations; challenges related to public vaccine confidence or awareness; uncertainties regarding the impact of COVID-19 on Pfizer’s business, operations and financial results; and competitive developments.</p>\n<p>A further description of risks and uncertainties can be found in Pfizer’s Annual Report on Form 10-K for the fiscal year ended December 31, 2020 and in its subsequent reports on Form 10-Q, including in the sections thereof captioned “Risk Factors” and “Forward-Looking Information and Factors That May Affect Future Results”, as well as in its subsequent reports on Form 8-K, all of which are filed with the U.S. Securities and Exchange Commission and available at <u>www.sec.gov</u> and <u>www.pfizer.com</u>.</p>\n<p><b>About BioNTech</b>Biopharmaceutical New Technologies is a next generation immunotherapy company pioneering novel therapies for cancer and other serious diseases. The Company exploits a wide array of computational discovery and therapeutic drug platforms for the rapid development of novel biopharmaceuticals. Its broad portfolio of oncology product candidates includes individualized and off-the-shelf mRNA-based therapies, innovative chimeric antigen receptor T cells, bi-specific checkpoint immuno-modulators, targeted cancer antibodies and small molecules. Based on its deep expertise in mRNA vaccine development and in-house manufacturing capabilities, BioNTech and its collaborators are developing multiple mRNA vaccine candidates for a range of infectious diseases alongside its diverse oncology pipeline. BioNTech has established a broad set of relationships with multiple global pharmaceutical collaborators, including Genmab, <a href=\"https://laohu8.com/S/GCVRZ\">Sanofi</a>, Bayer Animal Health, Genentech, a member of the Roche Group, Regeneron, Genevant, Fosun Pharma, and Pfizer. For more information, please visit <u>www.BioNTech.de</u>.</p>\n<p><b>BioNTech Forward-looking Statements</b>This press release contains “forward-looking statements” of BioNTech within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements may include, but may not be limited to, statements concerning: BioNTech’s efforts to combat COVID-19; the collaboration between BioNTech and Pfizer including the program to develop a COVID-19 vaccine and COMIRNATY (COVID-19 Vaccine, mRNA) (BNT162b2) (including a potential booster (third) dose of BNT162b2 in individuals 16 years of age and older in the U.S., a definite submission of a supplemental BLA for a potential booster dose of a variation of BNT162b2 having a modified mRNA sequence in the U.S., a BLA to support potential full FDA approval of BNT162b2 in individuals 12 through 15 years, whether and when applications for a potential booster (third) dose will be filed in any other jurisdictions, qualitative assessments of available data, potential benefits, expectations for clinical trials, the anticipated timing of regulatory submissions, regulatory approvals or authorizations and anticipated manufacturing, distribution and supply); our expectations regarding the potential characteristics of BNT162b2 in our clinical trials and/or in commercial use based on data observations to date; the ability of BNT162b2 to prevent COVID-19 caused by emerging virus variants; the expected time point for additional readouts on efficacy data of BNT162b2 in our clinical trials; the nature of the clinical data, which is subject to ongoing peer review, regulatory review and market interpretation; the timing for submission of data for, or receipt of, any marketing approval or Emergency Use Authorization; our contemplated shipping and storage plan, including our estimated product shelf life at various temperatures; and the ability of BioNTech to supply the quantities of BNT162 to support clinical development and market demand, including our production estimates for 2021. Any forward-looking statements in this press release are based on BioNTech current expectations and beliefs of future events, and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to: the ability to meet the pre-defined endpoints in clinical trials; competition to create a vaccine for COVID-19; the ability to produce comparable clinical or other results, including our stated rate of vaccine effectiveness and safety and tolerability profile observed to date, in the remainder of the trial or in larger, more diverse populations upon commercialization; the ability to effectively scale our productions capabilities; and other potential difficulties.</p>\n<p>For a discussion of these and other risks and uncertainties, see BioNTech’s Annual Report as Form 20-F for the Year Ended December 31, 2020, filed with the SEC on March 30, 2021, which is available on the SEC’s website at <u>www.sec.gov</u>. All information in this press release is as of the date of the release, and BioNTech undertakes no duty to update this information unless required by law.</p>","source":"highlight_streetinsider","collect":0,"html":"<!DOCTYPE html>\n<html>\n<head>\n<meta http-equiv=\"Content-Type\" content=\"text/html; charset=utf-8\" />\n<meta name=\"viewport\" content=\"width=device-width,initial-scale=1.0,minimum-scale=1.0,maximum-scale=1.0,user-scalable=no\"/>\n<meta name=\"format-detection\" content=\"telephone=no,email=no,address=no\" />\n<title>FDA Advisory Committee Votes Unanimously in Favor of COMIRNATY® Booster for Emergency Use in People 65 and Older and Certain High-Risk Populations</title>\n<style type=\"text/css\">\na,abbr,acronym,address,applet,article,aside,audio,b,big,blockquote,body,canvas,caption,center,cite,code,dd,del,details,dfn,div,dl,dt,\nem,embed,fieldset,figcaption,figure,footer,form,h1,h2,h3,h4,h5,h6,header,hgroup,html,i,iframe,img,ins,kbd,label,legend,li,mark,menu,nav,\nobject,ol,output,p,pre,q,ruby,s,samp,section,small,span,strike,strong,sub,summary,sup,table,tbody,td,tfoot,th,thead,time,tr,tt,u,ul,var,video{ font:inherit;margin:0;padding:0;vertical-align:baseline;border:0 }\nbody{ font-size:16px; line-height:1.5; color:#999; background:transparent; }\n.wrapper{ overflow:hidden;word-break:break-all;padding:10px; }\nh1,h2{ font-weight:normal; line-height:1.35; margin-bottom:.6em; }\nh3,h4,h5,h6{ line-height:1.35; margin-bottom:1em; }\nh1{ font-size:24px; }\nh2{ font-size:20px; }\nh3{ font-size:18px; }\nh4{ font-size:16px; }\nh5{ font-size:14px; }\nh6{ font-size:12px; }\np,ul,ol,blockquote,dl,table{ margin:1.2em 0; }\nul,ol{ margin-left:2em; }\nul{ list-style:disc; }\nol{ list-style:decimal; }\nli,li p{ margin:10px 0;}\nimg{ max-width:100%;display:block;margin:0 auto 1em; }\nblockquote{ color:#B5B2B1; border-left:3px solid #aaa; padding:1em; }\nstrong,b{font-weight:bold;}\nem,i{font-style:italic;}\ntable{ width:100%;border-collapse:collapse;border-spacing:1px;margin:1em 0;font-size:.9em; }\nth,td{ padding:5px;text-align:left;border:1px solid #aaa; }\nth{ font-weight:bold;background:#5d5d5d; }\n.symbol-link{font-weight:bold;}\n/* header{ border-bottom:1px solid #494756; } */\n.title{ margin:0 0 8px;line-height:1.3;color:#ddd; }\n.meta {color:#5e5c6d;font-size:13px;margin:0 0 .5em; }\na{text-decoration:none; color:#2a4b87;}\n.meta .head { display: inline-block; overflow: hidden}\n.head .h-thumb { width: 30px; height: 30px; margin: 0; padding: 0; border-radius: 50%; float: left;}\n.head .h-content { margin: 0; padding: 0 0 0 9px; float: left;}\n.head .h-name {font-size: 13px; color: #eee; margin: 0;}\n.head .h-time {font-size: 11px; color: #7E829C; margin: 0;line-height: 11px;}\n.small {font-size: 12.5px; display: inline-block; transform: scale(0.9); -webkit-transform: scale(0.9); transform-origin: left; -webkit-transform-origin: left;}\n.smaller {font-size: 12.5px; display: inline-block; transform: scale(0.8); -webkit-transform: scale(0.8); transform-origin: left; -webkit-transform-origin: left;}\n.bt-text {font-size: 12px;margin: 1.5em 0 0 0}\n.bt-text p {margin: 0}\n</style>\n</head>\n<body>\n<div class=\"wrapper\">\n<header>\n<h2 class=\"title\">\nFDA Advisory Committee Votes Unanimously in Favor of COMIRNATY® Booster for Emergency Use in People 65 and Older and Certain High-Risk Populations\n</h2>\n\n<h4 class=\"meta\">\n\n\n2021-09-18 15:40 GMT+8&nbsp;&nbsp;&nbsp;<a href=https://www.streetinsider.com/dr/news.php?id=18955632><strong>StreetInsider</strong></a>\n\n\n</h4>\n\n</header>\n<article>\n<div>\n<p>Committee reviewed clinical data showing a booster dose of COMIRNATY® elicits high neutralization titers against SARS-CoV-2 and all currently tested variants \nReactogenicity profile within seven days ...</p>\n\n<a href=\"https://www.streetinsider.com/dr/news.php?id=18955632\">Web Link</a>\n\n</div>\n\n\n</article>\n</div>\n</body>\n</html>\n","type":0,"thumbnail":"","relate_stocks":{"PFE":"辉瑞"},"source_url":"https://www.streetinsider.com/dr/news.php?id=18955632","is_english":true,"share_image_url":"https://static.laohu8.com/e9f99090a1c2ed51c021029395664489","article_id":"2168957763","content_text":"Committee reviewed clinical data showing a booster dose of COMIRNATY® elicits high neutralization titers against SARS-CoV-2 and all currently tested variants \nReactogenicity profile within seven days of the booster dose was typically mild to moderate, with frequency of reactions similar to or lower than after the primary vaccination series\nReal-world data presented by Israel Ministry of Health show additional protection after receiving a booster translated to vaccine effectiveness comparable to levels seen early in the country’s vaccine rollout\nFDA expected to make its decision in the coming days \n\nNEW YORK AND MAINZ, GERMANY, September 17, 2021—Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) announced today that the U.S. Food and Drug Administration’s (FDA) Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted unanimously to recommend the FDA grant Emergency Use Authorization (EUA) for a booster dose of COMIRNATY® (COVID-19 Vaccine, mRNA) in individuals 65 years of age and older and individuals at high risk of severe COVID-19. The committee recommended that the additional dose be administered at least six months after the two-dose series. The panel also agreed that healthcare workers and others at high risk for occupational exposure should be included in this EUA.\nVRBPAC is made up of independent experts who advise the FDA on scientific and regulatory matters, including the evaluation of vaccine safety and efficacy.\nAt this time, VRBPAC did not vote in favor of approval of a booster dose for the full population for which Pfizer and BioNTech submitted their supplemental Biologics License Application, which was individuals 16 and older. The same data have recently been submitted to the European Medicines Agency (EMA) and will be filed with other regulatory authorities in the coming weeks. The companies remain vigilant and continue to generate relevant COMIRNATY booster dose data for evaluation for future licensure in further groups as well as to address emerging variants of concern.\nThe FDA is expected to make its decision in the coming days. This decision could allow COMIRNATY to be the first COVID-19 vaccine with a booster authorized in the U.S.\n“Today the VRBPAC reviewed data from our clinical program showing a favorable safety profile and strong immune responses against SARS-CoV-2 after a booster dose of our vaccine. These data, and the larger body of scientific evidence presented at the meeting, underscore our belief that boosters can be a critical tool in the ongoing effort to control the spread of this virus,” said Kathrin U. Jansen, Ph.D., Senior Vice President and Head of Vaccine Research & Development, Pfizer. “We thank the committee for their thoughtful review of the data and will work with the FDA following today’s meeting to address the committee’s questions, as we continue to believe in the benefits of a booster dose for a broader population.”\n“We are committed to support the ongoing efforts to reduce infections and COVID-19 cases. The data we submitted to the FDA, EMA and other regulatory authorities underline that a booster induces a strong immune response against all tested variants of concern and may contribute to address a public health need,” said Özlem Türeci, M.D., Co-founder and Chief Medical Officer of BioNTech.\nVRBPAC based its recommendation on the totality of scientific evidence shared by the companies, including data from their clinical program evaluating the safety, tolerability and immunogenicity of a booster dose of COMIRNATY. A booster dose of the vaccine elicited significantly higher neutralizing antibody titers against the initial SARS-CoV-2 virus (wild type), as well as the Beta and Delta variants, when compared with the levels observed after the two-dose primary series. The reactogenicity profile within seven days after the booster dose was typically mild to moderate, and the frequency of reactions was similar to or lower than after dose two. The adverse event profile was generally consistent with other clinical safety data for COMIRNATY.\nReal-world surveillance data also were presented to the VRBPAC by the Israel Ministry of Health, providing further support for the public health impact of boosters. The data presented from Israel included an analysis published this week in The New England Journal of Medicine. The analysis comprised approximately 1.1 million individuals ages 60 years and older who were eligible for a booster dose of the vaccine between July 30 through August 31, 2021. No new safety signals were observed, and reported adverse events were lower than those observed after dose two. The analysis showed that a booster dose restored very high levels of protection against COVID-19 infections and severe disease in this period when Delta was the dominant strain. Individuals who received the booster dose were less likely by a factor of 11.3 (95% CI: 10.4, 12.3) to develop a confirmed infection and less likely by a factor of 19.5 (95% CI: 12.9, 29.5) to develop severe illness compared to those who were previously fully vaccinated but did not receive a booster dose. The additional protection after receiving a booster translated to vaccine effectiveness comparable to levels seen early in the country’s vaccine rollout (an estimated 95%), when the Alpha variant was predominant.\nUnder the EUA of the Pfizer-BioNTech vaccine in the U.S., a third dose was previously authorized for individuals at least 12 years of age who have undergone solid organ transplant, or who are diagnosed with conditions that are considered to have an equivalent level of immunocompromise. This authorization of a third dose for immunocompromised individuals is separate and distinct from the booster dose reviewed by VRBPAC today. The third dose for immunocompromised individuals is meant to address the fact that these individuals sometimes do not build enough protection after two doses of the vaccine. In contrast, the booster dose recommended today by VRBPAC for EUA refers to an additional dose of the vaccine that is given to those who have built enough protection after the primary two-dose vaccination series, but may have decreased protection over time due to waning of immunity.\nCOMIRNATY, which is based on BioNTech’s proprietary mRNA technology, was developed by both BioNTech and Pfizer. BioNTech is the Marketing Authorization Holder in the United States, the European Union, the United Kingdom, Canada and the holder of emergency use authorizations or equivalents in the United States (jointly with Pfizer) and other countries. Submissions to pursue regulatory approvals in those countries where emergency use authorizations or equivalent were initially granted are planned.\nU.S. Indication & Authorized UseCOMIRNATY® (COVID-19 Vaccine, mRNA) is an FDA-approved COVID-19 vaccine made by Pfizer for BioNTech.\n\nIt is approved as a 2-dose series for prevention of COVID-19 in individuals 16 years of age and older\nIt is also authorized under Emergency Use Authorization (EUA) to be administered for emergency use to:\n\nThe Pfizer-BioNTech COVID-19 Vaccine has received EUA from FDA to:\n\nprevent COVID-19 in individuals 12 years of age and older, and\nprovide a third dose to individuals 12 years of age and older who have been determined to have certain kinds of immunocompromise\n\nThe FDA-approved COMIRNATY® (COVID-19 Vaccine, mRNA) and the EUA-authorized Pfizer-BioNTech COVID-19 Vaccine have the same formulation and can be used interchangeably to provide the COVID-19 vaccination series. An individual may be offered either COMIRNATY® (COVID-19 Vaccine, mRNA) or the Pfizer-BioNTech COVID-19 Vaccine to prevent coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2.\nEUA StatementThis emergency use of the product has not been approved or licensed by FDA, but has been authorized by FDA under an Emergency Use Authorization (EUA) to prevent Coronavirus Disease 2019 (COVID-19) for use in individuals 12 years of age and older; and the emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of the medical product under Section 564(b)(1) of the FD&C Act unless the declaration is terminated or authorization revoked sooner.\nImportant Safety InformationIndividuals should not get the Pfizer-BioNTech COVID-19 Vaccine if they:\n\nhad a severe allergic reaction after a previous dose of this vaccine\nhad a severe allergic reaction to any ingredient of this vaccine\n\nIndividuals should tell the vaccination provider about all of their medical conditions, including if they:\n\nhave any allergies\nhave had myocarditis (inflammation of the heart muscle) or pericarditis (inflammation of the lining outside the heart)\nhave a fever\nhave a bleeding disorder or are on a blood thinner\nare immunocompromised or are on a medicine that affects the immune system\nare pregnant, plan to become pregnant, or are breastfeeding\nhave received another COVID-19 vaccine\nhave ever fainted in association with an injection\n\nThe vaccine may not protect everyone.\nSide effects reported with the vaccine include:\n\nThere is a remote chance that the vaccine could cause a severe allergic reaction\nMyocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the lining outside the heart) have occurred in some people who have received the vaccine. In most of these people, symptoms began within a few days following receipt of the second dose of the vaccine. The chance of having this occur is very low. Individuals should seek medical attention right away if they have any of the following symptoms after receiving the vaccine:\nSide effects that have been reported with the vaccine include:\nThese may not be all the possible side effects of the vaccine. Serious and unexpected side effects may occur. The vaccine is still being studied in clinical trials. Call the vaccination provider or healthcare provider about bothersome side effects or side effects that do not go away\n\nThere is no information on the use of the vaccine with other vaccines.\nPatients should always ask their healthcare providers for medical advice about adverse events. Individuals are encouraged to report negative side effects of vaccines to the US Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC). Visit http://www.vaers.hhs.gov or call 1-800-822-7967. In addition, side effects can be reported to Pfizer Inc. at www.pfizersafetyreporting.com or by calling 1-800-438-1985.\nPlease click here for full Prescribing Information (16+ years of age). Please click here for Fact Sheet for Vaccination Providers (12+ years of age).\nAbout Pfizer: Breakthroughs That Change Patients’ LivesAt Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products, including innovative medicines and vaccines. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as one of the world's premier innovative biopharmaceutical companies, we collaborate with health care providers, governments and local communities to support and expand access to reliable, affordable health care around the world. For more than 170 years, we have worked to make a difference for all who rely on us. We routinely post information that may be important to investors on our website at www.Pfizer.com. In addition, to learn more, please visit us on www.Pfizer.com and follow us on Twitter at @Pfizer and @Pfizer News, LinkedIn, YouTube and like us on Facebook at Facebook.com/Pfizer.\nPfizer Disclosure NoticeThe information contained in this release is as of September 17, 2021. Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments.\nThis release contains forward-looking information about Pfizer’s efforts to combat COVID-19, the collaboration between BioNTech and Pfizer to develop a COVID-19 vaccine, the BNT162 mRNA vaccine program and COMIRNATY (COVID-19 Vaccine, mRNA) (BNT162b2) (including a potential booster (third) dose and a supplemental Biologics License Application (sBLA) for a potential booster (third) dose of BNT162b2 in individuals 16 years of age and older in the U.S., qualitative assessments of available data, potential benefits, expectations for clinical trials, the anticipated timing of regulatory submissions, regulatory approvals or authorizations and anticipated manufacturing, distribution and supply) involving substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. Risks and uncertainties include, among other things, the uncertainties inherent in research and development, including the ability to meet anticipated clinical endpoints, commencement and/or completion dates for clinical trials, regulatory submission dates, regulatory approval dates and/or launch dates, as well as risks associated with preclinical and clinical data (including the Phase 3 data), including the possibility of unfavorable new preclinical, clinical or safety data and further analyses of existing preclinical, clinical or safety data; whether and when our Phase 3 clinical trial will demonstrate protection from infection or disease following a booster (third) dose, which is the subject of ongoing study; the ability to produce comparable clinical or other results, including the rate of vaccine effectiveness and safety and tolerability profile observed to date, in additional analyses of the Phase 3 trial and additional studies or in larger, more diverse populations following commercialization; the ability of BNT162b2 to prevent COVID-19 caused by emerging virus variants; the risk that more widespread use of the vaccine will lead to new information about efficacy, safety, or other developments, including the risk of additional adverse reactions, some of which may be serious; the risk that preclinical and clinical trial data are subject to differing interpretations and assessments, including during the peer review/publication process, in the scientific community generally, and by regulatory authorities; whether and when additional data from the BNT162 mRNA vaccine program will be published in scientific journal publications and, if so, when and with what modifications and interpretations; whether regulatory authorities will be satisfied with the design of and results from these and any future preclinical and clinical studies; whether and when applications for a potential booster (third) dose will be filed in any other jurisdictions and whether and when other biologics license and/or emergency use authorization applications or amendments to any such applications may be filed in particular jurisdictions for BNT162b2 or any other potential vaccines that may arise from the BNT162 program, and if obtained, whether or when such emergency use authorization or licenses will expire or terminate; whether and when any applications that may be pending or filed for BNT162b2 (including the sBLA for a potential booster (third) dose in the U.S., applications that may be pending or filed for a potential booster (third) dose in other jurisdictions or any requested amendments to the emergency use or conditional marketing authorizations) or other vaccines that may result from the BNT162 program may be approved by particular regulatory authorities, which will depend on myriad factors, including making a determination as to whether the vaccine’s benefits outweigh its known risks and determination of the vaccine’s efficacy and, if approved, whether it will be commercially successful; decisions by regulatory authorities impacting labeling or marketing, manufacturing processes, safety and/or other matters that could affect the availability or commercial potential of a vaccine, including development of products or therapies by other companies; disruptions in the relationships between us and our collaboration partners, clinical trial sites or third-party suppliers; the risk that demand for any products may be reduced or no longer exist; risks related to the availability of raw materials to manufacture a vaccine; challenges related to our vaccine’s ultra-low temperature formulation, two-dose schedule and attendant storage, distribution and administration requirements, including risks related to storage and handling after delivery by Pfizer; the risk that we may not be able to successfully develop other vaccine formulations, booster doses or new variant-specific vaccines; the risk that we may not be able to create or scale up manufacturing capacity on a timely basis or maintain access to logistics or supply channels commensurate with global demand for our vaccine, which would negatively impact our ability to supply the estimated numbers of doses of our vaccine within the projected time periods as previously indicated; whether and when additional supply agreements will be reached; uncertainties regarding the ability to obtain recommendations from vaccine advisory or technical committees and other public health authorities and uncertainties regarding the commercial impact of any such recommendations; challenges related to public vaccine confidence or awareness; uncertainties regarding the impact of COVID-19 on Pfizer’s business, operations and financial results; and competitive developments.\nA further description of risks and uncertainties can be found in Pfizer’s Annual Report on Form 10-K for the fiscal year ended December 31, 2020 and in its subsequent reports on Form 10-Q, including in the sections thereof captioned “Risk Factors” and “Forward-Looking Information and Factors That May Affect Future Results”, as well as in its subsequent reports on Form 8-K, all of which are filed with the U.S. Securities and Exchange Commission and available at www.sec.gov and www.pfizer.com.\nAbout BioNTechBiopharmaceutical New Technologies is a next generation immunotherapy company pioneering novel therapies for cancer and other serious diseases. The Company exploits a wide array of computational discovery and therapeutic drug platforms for the rapid development of novel biopharmaceuticals. Its broad portfolio of oncology product candidates includes individualized and off-the-shelf mRNA-based therapies, innovative chimeric antigen receptor T cells, bi-specific checkpoint immuno-modulators, targeted cancer antibodies and small molecules. Based on its deep expertise in mRNA vaccine development and in-house manufacturing capabilities, BioNTech and its collaborators are developing multiple mRNA vaccine candidates for a range of infectious diseases alongside its diverse oncology pipeline. BioNTech has established a broad set of relationships with multiple global pharmaceutical collaborators, including Genmab, Sanofi, Bayer Animal Health, Genentech, a member of the Roche Group, Regeneron, Genevant, Fosun Pharma, and Pfizer. For more information, please visit www.BioNTech.de.\nBioNTech Forward-looking StatementsThis press release contains “forward-looking statements” of BioNTech within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements may include, but may not be limited to, statements concerning: BioNTech’s efforts to combat COVID-19; the collaboration between BioNTech and Pfizer including the program to develop a COVID-19 vaccine and COMIRNATY (COVID-19 Vaccine, mRNA) (BNT162b2) (including a potential booster (third) dose of BNT162b2 in individuals 16 years of age and older in the U.S., a definite submission of a supplemental BLA for a potential booster dose of a variation of BNT162b2 having a modified mRNA sequence in the U.S., a BLA to support potential full FDA approval of BNT162b2 in individuals 12 through 15 years, whether and when applications for a potential booster (third) dose will be filed in any other jurisdictions, qualitative assessments of available data, potential benefits, expectations for clinical trials, the anticipated timing of regulatory submissions, regulatory approvals or authorizations and anticipated manufacturing, distribution and supply); our expectations regarding the potential characteristics of BNT162b2 in our clinical trials and/or in commercial use based on data observations to date; the ability of BNT162b2 to prevent COVID-19 caused by emerging virus variants; the expected time point for additional readouts on efficacy data of BNT162b2 in our clinical trials; the nature of the clinical data, which is subject to ongoing peer review, regulatory review and market interpretation; the timing for submission of data for, or receipt of, any marketing approval or Emergency Use Authorization; our contemplated shipping and storage plan, including our estimated product shelf life at various temperatures; and the ability of BioNTech to supply the quantities of BNT162 to support clinical development and market demand, including our production estimates for 2021. Any forward-looking statements in this press release are based on BioNTech current expectations and beliefs of future events, and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to: the ability to meet the pre-defined endpoints in clinical trials; competition to create a vaccine for COVID-19; the ability to produce comparable clinical or other results, including our stated rate of vaccine effectiveness and safety and tolerability profile observed to date, in the remainder of the trial or in larger, more diverse populations upon commercialization; the ability to effectively scale our productions capabilities; and other potential difficulties.\nFor a discussion of these and other risks and uncertainties, see BioNTech’s Annual Report as Form 20-F for the Year Ended December 31, 2020, filed with the SEC on March 30, 2021, which is available on the SEC’s website at www.sec.gov. All information in this press release is as of the date of the release, and BioNTech undertakes no duty to update this information unless required by law.","news_type":1},"isVote":1,"tweetType":1,"viewCount":797,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"EN","totalScore":0},{"id":834592172,"gmtCreate":1629812270596,"gmtModify":1676530138996,"author":{"id":"3577522329316309","authorId":"3577522329316309","name":"pompeepee","avatar":"https://static.laohu8.com/default-avatar.jpg","crmLevel":2,"crmLevelSwitch":0,"followedFlag":false,"idStr":"3577522329316309","authorIdStr":"3577522329316309"},"themes":[],"htmlText":"whee","listText":"whee","text":"whee","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":2,"commentSize":1,"repostSize":0,"link":"https://ttm.financial/post/834592172","repostId":"1154386229","repostType":4,"isVote":1,"tweetType":1,"viewCount":598,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"EN","totalScore":0},{"id":831136474,"gmtCreate":1629294304098,"gmtModify":1676529994455,"author":{"id":"3577522329316309","authorId":"3577522329316309","name":"pompeepee","avatar":"https://static.laohu8.com/default-avatar.jpg","crmLevel":2,"crmLevelSwitch":0,"followedFlag":false,"idStr":"3577522329316309","authorIdStr":"3577522329316309"},"themes":[],"htmlText":"wa","listText":"wa","text":"wa","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":2,"commentSize":1,"repostSize":0,"link":"https://ttm.financial/post/831136474","repostId":"2160735178","repostType":4,"repost":{"id":"2160735178","kind":"highlight","pubTimestamp":1629292500,"share":"https://ttm.financial/m/news/2160735178?lang=&edition=fundamental","pubTime":"2021-08-18 21:15","market":"us","language":"en","title":"3 Stocks Warren Buffett Is Selling That You Should Be Buying Hand Over Fist","url":"https://stock-news.laohu8.com/highlight/detail?id=2160735178","media":"Motley Fool","summary":"Berkshire Hathaway's stakes in these top-tier companies were reduced during the second quarter.","content":"<p>When it comes to investing prowess, Warren Buffett is in a class of his own. Since taking the helm of conglomerate <b>Berkshire Hathaway</b> (NYSE:BRK.A)(NYSE:BRK.B) in 1965, he's helped deliver an average annual return to shareholders of 20%. That's 56 years and an <i>average annual return of 20% </i>over those 56 years! Taking into account the year-to-date gain from the Class A shares (BRK.A), Buffett has overseen a nearly 3,400,000% return in Berkshire Hathaway's stock while CEO.</p>\n<p>Suffice it to say, when Warren Buffett buys, adds to, reduces, or sells out of a stock, Wall Street and the investing community pay very close attention. On Monday, Aug. 16, investors received their latest peek under the hood.</p>\n<p><img src=\"https://static.tigerbbs.com/1077c8372814d2b8150e933b4c608005\" tg-width=\"700\" tg-height=\"466\" referrerpolicy=\"no-referrer\" width=\"100%\" height=\"auto\"></p>\n<p>Berkshire Hathaway CEO Warren Buffett. Image source: The Motley Fool.</p>\n<h3>Berkshire Hathaway was a net-seller of stocks in Q2</h3>\n<p>Companies and individuals managing at least $100 million in assets are required to file Form 13F with the Securities and Exchange Commission 45 days after a quarter has ended. A 13F provides a (dated) snapshot of what institutional investors, hedge funds, or market mavens were holding as of the end of the most recent quarter (June 30).</p>\n<p>Berkshire Hathaway's latest 13F showed a considerable amount of selling, rather than buying. In total, four stocks were purchased or added to during the second quarter, with the biggest buy being grocery chain <b>Kroger</b>. More than 10.7 million shares were added, boosting Berkshire Hathaway's stake to almost 61.8 million shares.</p>\n<p>On the other hand, 11 stocks were reduced or completely given the heave-ho. <b>Axalta Coating Systems</b>, Berkshire Hathaway's only exposure to the materials sector, was completely sold. Additionally, the Oracle of Omaha and his investing team sent <b>Biogen</b>&nbsp;and <b><a href=\"https://laohu8.com/S/LFG.AU\">Liberty</a> Global </b>(Class A, LBTYA) packing. Note, Berkshire still owns a reduced stake in <b>Liberty Global</b>'s Class C shares (LBTYK).</p>\n<p>But among the eight other holdings that were reduced are three stocks that investors should be buying hand over fist. Buffett and his investing lieutenants may have an impressive track record, but they're not infallible.</p>\n<p><img src=\"https://static.tigerbbs.com/fe7d1b8c040ec63440ca65517ac114c2\" tg-width=\"700\" tg-height=\"466\" referrerpolicy=\"no-referrer\" width=\"100%\" height=\"auto\"></p>\n<p>The all-electric 2022 Chevrolet Bolt EUV. Image source: General Motors.</p>\n<h3>General Motors</h3>\n<p>First up is auto stock <b>General Motors</b> (NYSE:GM), which has been consistently trimmed in recent quarters. During the second quarter, Buffett and his team reduced Berkshire's GM stake by 7 million shares, leaving the company with 60 million shares.</p>\n<p>Why reduce the General Motors stake? One possibility is persistent supply chain disruption caused by the coronavirus pandemic. Chip shortages have caused automakers to halt or reduce production of certain models, which should adversely affect their operating performance in the near term.</p>\n<p>Another possible reason Buffett or his investing lieutenants, Todd Combs and Ted Weschler, may have chosen to lighten the load is GM's valuation. Since emerging from bankruptcy over a decade ago, GM's market cap was never higher than it was during the second quarter (a peak of $92 billion).</p>\n<p>But whatever the reasoning is, selling shares of General Motors isn't a smart move. If anything, General Motors is more attractive now than it's been in over a decade. That's because it's going to benefit from a multi-decade vehicle replacement cycle as consumers and enterprises go electric.</p>\n<p>In mid-June, General Motors announced its plans to up spending on electric vehicles (EV), autonomous vehicles, and battery technology to $35 billion through 2025. That's a 75% increase from its previous spending commitment on clean-energy solutions from prior to the pandemic. The expectation is that GM will launch 30 new EVs worldwide by mid-decade.</p>\n<p>General Motors also has significant inroads in China, the world's largest auto market. With a number of established brands in the Chinese market and the infrastructure necessary to ramp up production, GM shouldn't have any issue gobbling up EV market share.</p>\n<p>Currently valued at less than 8 times Wall Street's earnings-per-share forecast for 2022, GM is a screaming buy.</p>\n<p><img src=\"https://g.foolcdn.com/image/?url=https%3A%2F%2Fg.foolcdn.com%2Feditorial%2Fimages%2F639553%2Fusb-mobile-app.jpg&amp;w=700&amp;op=resize\" tg-width=\"700\" tg-height=\"466\" referrerpolicy=\"no-referrer\" width=\"100%\" height=\"auto\"></p>\n<p>Image source: U.S. Bank (U.S. Bancorp is U.S. Bank's parent company).</p>\n<h3>U.S. Bancorp</h3>\n<p>Another surefire winner that was, once again, reduced very modestly by Buffett and his team during the quarter is regional bank stock <b>U.S. Bancorp</b> (NYSE:USB). In total, 798,178 shares were sold, equating to a 0.6% reduction from its first-quarter stake. All told, Berkshire Hathaway still holds almost 128.9 million shares of U.S. Bancorp.</p>\n<p>If you're looking for a valid reason why 798,178 shares were sold during the second quarter, the best guess I can offer is Berkshire Hathaway wanting to keep away from the 10% ownership threshold for banks that would qualify it as a bank holding company (BHC). As a BHC, Berkshire's reporting and trading activity would be considerably more stringent than it is now. Perhaps Buffett was anticipating Berkshire's stake in U.S. Bancorp growing due to future buybacks.</p>\n<p>But like GM, it really doesn't matter why Buffett sold. Right now, U.S. Bancorp is <a href=\"https://laohu8.com/S/AONE.U\">one</a> of the most attractive bank stocks investors can buy.</p>\n<p>To start with, it's consistently near the top or leading big banks in return on assets (ROA). Whereas most banks strive for a 1% ROA, U.S. Bancorp has a knack for delivering a 1.6% ROA, which is indicative of its fantastic management team. This is a company that's stuck true to the bread-and-butter of banking (i.e., loan and deposit growth), and has generally avoided the riskier derivative investment opportunities that ravaged money-center banks during the Great Recession.</p>\n<p>Furthermore, U.S. Bancorp is a banking leader when it comes to digital adoption. Approximately 79% of its customers were active digitally (online or mobile) in the May-ended quarter, which is up 7 percentage points from the comparable quarter two years prior. What's more, nearly two-thirds of all loan sales were completed online or via mobile app since 2021 began.</p>\n<p>As one of the nation's most efficient banks, U.S. Bancorp is set to thrive as the U.S. economic recovery takes shape.</p>\n<p><img src=\"https://g.foolcdn.com/image/?url=https%3A%2F%2Fg.foolcdn.com%2Feditorial%2Fimages%2F639553%2Fbiotech-lab-research-with-multiple-pipettes-getty.jpg&amp;w=700&amp;op=resize\" tg-width=\"700\" tg-height=\"466\" referrerpolicy=\"no-referrer\" width=\"100%\" height=\"auto\"></p>\n<p>Image source: Getty Images.</p>\n<h3>Bristol Myers Squibb</h3>\n<p>A third stock Berkshire Hathaway reduced in the second quarter is pharmaceutical giant <b>Bristol Myers Squibb</b> (NYSE:BMY). A little over 4.7 million shares were sold, which ultimately reduced Buffett's company's stake by 15% to roughly 26.3 million shares.</p>\n<p>Before diving into the \"why?\" part of the selling process, it's important to note that this position is almost certainly the responsibility of Buffett's investing lieutenants. The Oracle of Omaha has never had the interest or energy to keep up with clinical trials, which is a big reason he's generally avoided drugmakers over the years.</p>\n<p>As for why the Bristol Myers position was cut by 15%, there are two possible explanations. First, the company has stalled out around $70 a share on two previous occasions (1999 and 2016). With the company pushing back into the mid-$60 range in the second quarter, perhaps Combs and Weschler felt it was a prudent time to lock in some gains.</p>\n<p>The second possibility is that Bristol Myers Squibb was purchased as a coronavirus play, and it simply hasn't materialized as one.</p>\n<p>Not to sound like a broken record, but whatever the reasoning is, selling Bristol Myers Squibb at less than 9 times forward-year earnings is a mistake. This is a healthcare stock investors should be buying hand over fist.</p>\n<p>On the organic growth front, Bristol Myers is making waves. Eliquis, which was developed in combination with <b>Pfizer</b>, has become the leading oral anticoagulant and is on track for more than $10 billion in annual sales. Meanwhile, cancer immunotherapy Opdivo brought in $7 billion last year and is being examined in dozens of clinical trials as a monotherapy or combination treatment. Label expansion opportunities offer ample upside for Opdivo.</p>\n<p>Bristol Myers Squibb also turned heads with its 2019 acquisition of cancer and immunology drugmaker Celgene. Buying Celgene brought one of the world's top-selling cancer drugs, Revlimid, into the fold. Revlimid's annual sales have grown by a double-digit percentage for more than a decade, with the multiple myeloma drug benefiting from improved cancer-screening diagnostics, strong pricing power, increased duration of use, and label expansions. Since it's protected from a flood of generic competition until February 2026, Bristol Myers has a long runway to reap the rewards of its new cash cow.</p>","source":"fool_stock","collect":0,"html":"<!DOCTYPE html>\n<html>\n<head>\n<meta http-equiv=\"Content-Type\" content=\"text/html; charset=utf-8\" />\n<meta name=\"viewport\" content=\"width=device-width,initial-scale=1.0,minimum-scale=1.0,maximum-scale=1.0,user-scalable=no\"/>\n<meta name=\"format-detection\" content=\"telephone=no,email=no,address=no\" />\n<title>3 Stocks Warren Buffett Is Selling That You Should Be Buying Hand Over Fist</title>\n<style type=\"text/css\">\na,abbr,acronym,address,applet,article,aside,audio,b,big,blockquote,body,canvas,caption,center,cite,code,dd,del,details,dfn,div,dl,dt,\nem,embed,fieldset,figcaption,figure,footer,form,h1,h2,h3,h4,h5,h6,header,hgroup,html,i,iframe,img,ins,kbd,label,legend,li,mark,menu,nav,\nobject,ol,output,p,pre,q,ruby,s,samp,section,small,span,strike,strong,sub,summary,sup,table,tbody,td,tfoot,th,thead,time,tr,tt,u,ul,var,video{ font:inherit;margin:0;padding:0;vertical-align:baseline;border:0 }\nbody{ font-size:16px; line-height:1.5; color:#999; background:transparent; }\n.wrapper{ overflow:hidden;word-break:break-all;padding:10px; }\nh1,h2{ font-weight:normal; line-height:1.35; margin-bottom:.6em; }\nh3,h4,h5,h6{ line-height:1.35; margin-bottom:1em; }\nh1{ font-size:24px; }\nh2{ font-size:20px; }\nh3{ font-size:18px; }\nh4{ font-size:16px; }\nh5{ font-size:14px; }\nh6{ font-size:12px; }\np,ul,ol,blockquote,dl,table{ margin:1.2em 0; }\nul,ol{ margin-left:2em; }\nul{ list-style:disc; }\nol{ list-style:decimal; }\nli,li p{ margin:10px 0;}\nimg{ max-width:100%;display:block;margin:0 auto 1em; }\nblockquote{ color:#B5B2B1; border-left:3px solid #aaa; padding:1em; }\nstrong,b{font-weight:bold;}\nem,i{font-style:italic;}\ntable{ width:100%;border-collapse:collapse;border-spacing:1px;margin:1em 0;font-size:.9em; }\nth,td{ padding:5px;text-align:left;border:1px solid #aaa; }\nth{ font-weight:bold;background:#5d5d5d; }\n.symbol-link{font-weight:bold;}\n/* header{ border-bottom:1px solid #494756; } */\n.title{ margin:0 0 8px;line-height:1.3;color:#ddd; }\n.meta {color:#5e5c6d;font-size:13px;margin:0 0 .5em; }\na{text-decoration:none; color:#2a4b87;}\n.meta .head { display: inline-block; overflow: hidden}\n.head .h-thumb { width: 30px; height: 30px; margin: 0; padding: 0; border-radius: 50%; float: left;}\n.head .h-content { margin: 0; padding: 0 0 0 9px; float: left;}\n.head .h-name {font-size: 13px; color: #eee; margin: 0;}\n.head .h-time {font-size: 11px; color: #7E829C; margin: 0;line-height: 11px;}\n.small {font-size: 12.5px; display: inline-block; transform: scale(0.9); -webkit-transform: scale(0.9); transform-origin: left; -webkit-transform-origin: left;}\n.smaller {font-size: 12.5px; display: inline-block; transform: scale(0.8); -webkit-transform: scale(0.8); transform-origin: left; -webkit-transform-origin: left;}\n.bt-text {font-size: 12px;margin: 1.5em 0 0 0}\n.bt-text p {margin: 0}\n</style>\n</head>\n<body>\n<div class=\"wrapper\">\n<header>\n<h2 class=\"title\">\n3 Stocks Warren Buffett Is Selling That You Should Be Buying Hand Over Fist\n</h2>\n\n<h4 class=\"meta\">\n\n\n2021-08-18 21:15 GMT+8&nbsp;&nbsp;&nbsp;<a href=https://www.fool.com/investing/2021/08/18/3-stocks-buffett-is-selling-you-should-be-buying/><strong>Motley Fool</strong></a>\n\n\n</h4>\n\n</header>\n<article>\n<div>\n<p>When it comes to investing prowess, Warren Buffett is in a class of his own. Since taking the helm of conglomerate Berkshire Hathaway (NYSE:BRK.A)(NYSE:BRK.B) in 1965, he's helped deliver an average ...</p>\n\n<a href=\"https://www.fool.com/investing/2021/08/18/3-stocks-buffett-is-selling-you-should-be-buying/\">Web Link</a>\n\n</div>\n\n\n</article>\n</div>\n</body>\n</html>\n","type":0,"thumbnail":"","relate_stocks":{"BRK.B":"伯克希尔B","USB":"美国合众银行","GM":"通用汽车","BRK.A":"伯克希尔"},"source_url":"https://www.fool.com/investing/2021/08/18/3-stocks-buffett-is-selling-you-should-be-buying/","is_english":true,"share_image_url":"https://static.laohu8.com/e9f99090a1c2ed51c021029395664489","article_id":"2160735178","content_text":"When it comes to investing prowess, Warren Buffett is in a class of his own. Since taking the helm of conglomerate Berkshire Hathaway (NYSE:BRK.A)(NYSE:BRK.B) in 1965, he's helped deliver an average annual return to shareholders of 20%. That's 56 years and an average annual return of 20% over those 56 years! Taking into account the year-to-date gain from the Class A shares (BRK.A), Buffett has overseen a nearly 3,400,000% return in Berkshire Hathaway's stock while CEO.\nSuffice it to say, when Warren Buffett buys, adds to, reduces, or sells out of a stock, Wall Street and the investing community pay very close attention. On Monday, Aug. 16, investors received their latest peek under the hood.\n\nBerkshire Hathaway CEO Warren Buffett. Image source: The Motley Fool.\nBerkshire Hathaway was a net-seller of stocks in Q2\nCompanies and individuals managing at least $100 million in assets are required to file Form 13F with the Securities and Exchange Commission 45 days after a quarter has ended. A 13F provides a (dated) snapshot of what institutional investors, hedge funds, or market mavens were holding as of the end of the most recent quarter (June 30).\nBerkshire Hathaway's latest 13F showed a considerable amount of selling, rather than buying. In total, four stocks were purchased or added to during the second quarter, with the biggest buy being grocery chain Kroger. More than 10.7 million shares were added, boosting Berkshire Hathaway's stake to almost 61.8 million shares.\nOn the other hand, 11 stocks were reduced or completely given the heave-ho. Axalta Coating Systems, Berkshire Hathaway's only exposure to the materials sector, was completely sold. Additionally, the Oracle of Omaha and his investing team sent Biogen and Liberty Global (Class A, LBTYA) packing. Note, Berkshire still owns a reduced stake in Liberty Global's Class C shares (LBTYK).\nBut among the eight other holdings that were reduced are three stocks that investors should be buying hand over fist. Buffett and his investing lieutenants may have an impressive track record, but they're not infallible.\n\nThe all-electric 2022 Chevrolet Bolt EUV. Image source: General Motors.\nGeneral Motors\nFirst up is auto stock General Motors (NYSE:GM), which has been consistently trimmed in recent quarters. During the second quarter, Buffett and his team reduced Berkshire's GM stake by 7 million shares, leaving the company with 60 million shares.\nWhy reduce the General Motors stake? One possibility is persistent supply chain disruption caused by the coronavirus pandemic. Chip shortages have caused automakers to halt or reduce production of certain models, which should adversely affect their operating performance in the near term.\nAnother possible reason Buffett or his investing lieutenants, Todd Combs and Ted Weschler, may have chosen to lighten the load is GM's valuation. Since emerging from bankruptcy over a decade ago, GM's market cap was never higher than it was during the second quarter (a peak of $92 billion).\nBut whatever the reasoning is, selling shares of General Motors isn't a smart move. If anything, General Motors is more attractive now than it's been in over a decade. That's because it's going to benefit from a multi-decade vehicle replacement cycle as consumers and enterprises go electric.\nIn mid-June, General Motors announced its plans to up spending on electric vehicles (EV), autonomous vehicles, and battery technology to $35 billion through 2025. That's a 75% increase from its previous spending commitment on clean-energy solutions from prior to the pandemic. The expectation is that GM will launch 30 new EVs worldwide by mid-decade.\nGeneral Motors also has significant inroads in China, the world's largest auto market. With a number of established brands in the Chinese market and the infrastructure necessary to ramp up production, GM shouldn't have any issue gobbling up EV market share.\nCurrently valued at less than 8 times Wall Street's earnings-per-share forecast for 2022, GM is a screaming buy.\n\nImage source: U.S. Bank (U.S. Bancorp is U.S. Bank's parent company).\nU.S. Bancorp\nAnother surefire winner that was, once again, reduced very modestly by Buffett and his team during the quarter is regional bank stock U.S. Bancorp (NYSE:USB). In total, 798,178 shares were sold, equating to a 0.6% reduction from its first-quarter stake. All told, Berkshire Hathaway still holds almost 128.9 million shares of U.S. Bancorp.\nIf you're looking for a valid reason why 798,178 shares were sold during the second quarter, the best guess I can offer is Berkshire Hathaway wanting to keep away from the 10% ownership threshold for banks that would qualify it as a bank holding company (BHC). As a BHC, Berkshire's reporting and trading activity would be considerably more stringent than it is now. Perhaps Buffett was anticipating Berkshire's stake in U.S. Bancorp growing due to future buybacks.\nBut like GM, it really doesn't matter why Buffett sold. Right now, U.S. Bancorp is one of the most attractive bank stocks investors can buy.\nTo start with, it's consistently near the top or leading big banks in return on assets (ROA). Whereas most banks strive for a 1% ROA, U.S. Bancorp has a knack for delivering a 1.6% ROA, which is indicative of its fantastic management team. This is a company that's stuck true to the bread-and-butter of banking (i.e., loan and deposit growth), and has generally avoided the riskier derivative investment opportunities that ravaged money-center banks during the Great Recession.\nFurthermore, U.S. Bancorp is a banking leader when it comes to digital adoption. Approximately 79% of its customers were active digitally (online or mobile) in the May-ended quarter, which is up 7 percentage points from the comparable quarter two years prior. What's more, nearly two-thirds of all loan sales were completed online or via mobile app since 2021 began.\nAs one of the nation's most efficient banks, U.S. Bancorp is set to thrive as the U.S. economic recovery takes shape.\n\nImage source: Getty Images.\nBristol Myers Squibb\nA third stock Berkshire Hathaway reduced in the second quarter is pharmaceutical giant Bristol Myers Squibb (NYSE:BMY). A little over 4.7 million shares were sold, which ultimately reduced Buffett's company's stake by 15% to roughly 26.3 million shares.\nBefore diving into the \"why?\" part of the selling process, it's important to note that this position is almost certainly the responsibility of Buffett's investing lieutenants. The Oracle of Omaha has never had the interest or energy to keep up with clinical trials, which is a big reason he's generally avoided drugmakers over the years.\nAs for why the Bristol Myers position was cut by 15%, there are two possible explanations. First, the company has stalled out around $70 a share on two previous occasions (1999 and 2016). With the company pushing back into the mid-$60 range in the second quarter, perhaps Combs and Weschler felt it was a prudent time to lock in some gains.\nThe second possibility is that Bristol Myers Squibb was purchased as a coronavirus play, and it simply hasn't materialized as one.\nNot to sound like a broken record, but whatever the reasoning is, selling Bristol Myers Squibb at less than 9 times forward-year earnings is a mistake. This is a healthcare stock investors should be buying hand over fist.\nOn the organic growth front, Bristol Myers is making waves. Eliquis, which was developed in combination with Pfizer, has become the leading oral anticoagulant and is on track for more than $10 billion in annual sales. Meanwhile, cancer immunotherapy Opdivo brought in $7 billion last year and is being examined in dozens of clinical trials as a monotherapy or combination treatment. Label expansion opportunities offer ample upside for Opdivo.\nBristol Myers Squibb also turned heads with its 2019 acquisition of cancer and immunology drugmaker Celgene. Buying Celgene brought one of the world's top-selling cancer drugs, Revlimid, into the fold. Revlimid's annual sales have grown by a double-digit percentage for more than a decade, with the multiple myeloma drug benefiting from improved cancer-screening diagnostics, strong pricing power, increased duration of use, and label expansions. Since it's protected from a flood of generic competition until February 2026, Bristol Myers has a long runway to reap the rewards of its new cash cow.","news_type":1},"isVote":1,"tweetType":1,"viewCount":781,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"EN","totalScore":0},{"id":892488985,"gmtCreate":1628683856647,"gmtModify":1676529819573,"author":{"id":"3577522329316309","authorId":"3577522329316309","name":"pompeepee","avatar":"https://static.laohu8.com/default-avatar.jpg","crmLevel":2,"crmLevelSwitch":0,"followedFlag":false,"idStr":"3577522329316309","authorIdStr":"3577522329316309"},"themes":[],"htmlText":"wow","listText":"wow","text":"wow","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":2,"commentSize":1,"repostSize":0,"link":"https://ttm.financial/post/892488985","repostId":"2158186289","repostType":4,"isVote":1,"tweetType":1,"viewCount":889,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"EN","totalScore":0},{"id":898399845,"gmtCreate":1628472161587,"gmtModify":1703506532360,"author":{"id":"3577522329316309","authorId":"3577522329316309","name":"pompeepee","avatar":"https://static.laohu8.com/default-avatar.jpg","crmLevel":2,"crmLevelSwitch":0,"followedFlag":false,"idStr":"3577522329316309","authorIdStr":"3577522329316309"},"themes":[],"htmlText":"likee","listText":"likee","text":"likee","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":6,"commentSize":0,"repostSize":0,"link":"https://ttm.financial/post/898399845","repostId":"1136322726","repostType":4,"isVote":1,"tweetType":1,"viewCount":396,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"EN","totalScore":0},{"id":891155674,"gmtCreate":1628354217998,"gmtModify":1703505363883,"author":{"id":"3577522329316309","authorId":"3577522329316309","name":"pompeepee","avatar":"https://static.laohu8.com/default-avatar.jpg","crmLevel":2,"crmLevelSwitch":0,"followedFlag":false,"idStr":"3577522329316309","authorIdStr":"3577522329316309"},"themes":[],"htmlText":"yay","listText":"yay","text":"yay","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":0,"commentSize":1,"repostSize":0,"link":"https://ttm.financial/post/891155674","repostId":"1139912651","repostType":4,"isVote":1,"tweetType":1,"viewCount":758,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"EN","totalScore":0},{"id":893155774,"gmtCreate":1628249746898,"gmtModify":1703503933690,"author":{"id":"3577522329316309","authorId":"3577522329316309","name":"pompeepee","avatar":"https://static.laohu8.com/default-avatar.jpg","crmLevel":2,"crmLevelSwitch":0,"followedFlag":false,"idStr":"3577522329316309","authorIdStr":"3577522329316309"},"themes":[],"htmlText":"yay","listText":"yay","text":"yay","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":1,"commentSize":1,"repostSize":0,"link":"https://ttm.financial/post/893155774","repostId":"1180256775","repostType":4,"isVote":1,"tweetType":1,"viewCount":794,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"EN","totalScore":0},{"id":804774234,"gmtCreate":1627985070728,"gmtModify":1703499099220,"author":{"id":"3577522329316309","authorId":"3577522329316309","name":"pompeepee","avatar":"https://static.laohu8.com/default-avatar.jpg","crmLevel":2,"crmLevelSwitch":0,"followedFlag":false,"idStr":"3577522329316309","authorIdStr":"3577522329316309"},"themes":[],"htmlText":"wah","listText":"wah","text":"wah","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":5,"commentSize":0,"repostSize":0,"link":"https://ttm.financial/post/804774234","repostId":"2156100119","repostType":4,"repost":{"id":"2156100119","kind":"highlight","weMediaInfo":{"introduction":"Dow Jones publishes the world’s most trusted business news and financial information in a variety of media.","home_visible":0,"media_name":"Dow Jones","id":"106","head_image":"https://static.tigerbbs.com/150f88aa4d182df19190059f4a365e99"},"pubTimestamp":1627983900,"share":"https://ttm.financial/m/news/2156100119?lang=&edition=fundamental","pubTime":"2021-08-03 17:45","market":"us","language":"en","title":"August is among the worst months of year for the stock market. Here's how to play it.","url":"https://stock-news.laohu8.com/highlight/detail?id=2156100119","media":"Dow Jones","summary":"On Wall Street, August is off to a solid start, but the month tends to accompany a bout of turbulenc","content":"<p>On Wall Street, August is off to a solid start, but the month tends to accompany a bout of turbulence in equity markets.</p>\n<p>The month is associated with the worst performances for the Dow Jones Industrial Average , S&amp;P 500 index , as well as the small cap Russell 2000 and large-cap Russell1000 indexes, over the past three decades, according to the folks at Stock Trader's Almanac.</p>\n<p>The research outfit said that from 1988 to 2020 average declines for the benchmarks ranged from 0.4% for the Russell 2000 to 0.8% by Dow. For the Nasdaq Composite, meanwhile, August ranks as second-worst, with an average gain of 0.2% over the same period, with September being the worst month for the technology-heavy index.</p>\n<p>To be sure, a year ago, in the midst of the COVID-19 pandemic, August produced stellar returns across the board as investors bet on an eventual rebound in pandemic-plagued markets.</p>\n<p>However, last year's uncharacteristically strong performance, which saw monthly gains of over 9% for the Nasdaq Composite and over 7% for the Dow and S&amp;P 500, doesn't mean the long-term trend has changed.</p>\n<p>\"As shown in the LPL Chart of the Day, August and September have been historically two of the weakest months of the year,\" wrote Ryan Detrick, chief market strategist for LPL Financial, in a Monday research note.</p>\n<p>Check out the monthly returns on average since 1950:</p>\n<p>Here are the historical rankings by month via LPL:</p>\n<p>The folks at Bespoke Investment Group put a finer point on the underperformance for August, especially after a strong year-to-date performance, as has been enjoyed in 2021.</p>\n<p>\"Since 1983, the weakest August returns tend to come in years where the S&amp;P 500 was up over 10% YTD heading into the month,\" the researchers note.</p>\n<p>The markets performance thus far has come on the back of stellar earnings results as American corporations rebound from COVID-19, but there are lingering fears that the U.S. has reached or is near peak earnings and economic growth .</p>\n<p><b>So how to play the turbulent stretch?</b></p>\n<p>Jeff Hirsch, editor of the Stock Trader's Almanac, said that the first nine trading days of August tend to be the most prone to weakness while the rest of the month is better. That said, he warns that the expirations of futures and options contracts toward the end of the month tend to create a fresh bout of chop in August, heading toward September, another rough patch for stocks.</p>\n<p>\"The end of August tends to be weaker when traders evacuate Wall Street for the summer finale,\" Hirsch wrote.</p>\n<p>\"Expiration week is down more than half the time since 1990, with some sizable losses,\" he said.</p>\n<p>Stock Trader's Almanac indicated that bullishness prevails in the market, however. \"Bullish forces continue to persist. The Fed remains easy and accommodative. More fiscal stimulus is likely from Washington as Congress nears finalizing the deals on infrastructure and spending,\" the data company wrote. But it cautioned that outperforming second-quarter earnings and the spread of the Delta variant of COVID-19 \"is a concern and poses a threat to the bull and the economic expansion.\"</p>\n<p>\"Political wrangling here in the States and geopolitical machinations around world could also knock the market off course momentarily,\" Stock Trader's Almanac wrote, while noting that its outlook for the S&amp;P 500 sees a push to the 4500-4600 range or even higher.</p>\n<p>Strategists continue to recommend investment prudence, especially with the benchmark 10-year Treasury yields hanging around a multi-month low near 1.15%.</p>\n<p>Bespoke Investment Group also points to a strong 2021, even if the next two months are a bit bumpy, noting that that final stretch of the year tends to be strong when the months leading up to August also have been healthy.</p>\n<p>\"While the average and median returns for August may be lackluster, the final four months of the year have seen an average gain of 5.94% (median: 8.03%) with gains 12 out of 14 times (85%). That's pretty consistent,\" the analysts wrote.</p>","collect":0,"html":"<!DOCTYPE html>\n<html>\n<head>\n<meta http-equiv=\"Content-Type\" content=\"text/html; charset=utf-8\" />\n<meta name=\"viewport\" content=\"width=device-width,initial-scale=1.0,minimum-scale=1.0,maximum-scale=1.0,user-scalable=no\"/>\n<meta name=\"format-detection\" content=\"telephone=no,email=no,address=no\" />\n<title>August is among the worst months of year for the stock market. Here's how to play it.</title>\n<style type=\"text/css\">\na,abbr,acronym,address,applet,article,aside,audio,b,big,blockquote,body,canvas,caption,center,cite,code,dd,del,details,dfn,div,dl,dt,\nem,embed,fieldset,figcaption,figure,footer,form,h1,h2,h3,h4,h5,h6,header,hgroup,html,i,iframe,img,ins,kbd,label,legend,li,mark,menu,nav,\nobject,ol,output,p,pre,q,ruby,s,samp,section,small,span,strike,strong,sub,summary,sup,table,tbody,td,tfoot,th,thead,time,tr,tt,u,ul,var,video{ font:inherit;margin:0;padding:0;vertical-align:baseline;border:0 }\nbody{ font-size:16px; line-height:1.5; color:#999; background:transparent; }\n.wrapper{ overflow:hidden;word-break:break-all;padding:10px; }\nh1,h2{ font-weight:normal; line-height:1.35; margin-bottom:.6em; }\nh3,h4,h5,h6{ line-height:1.35; margin-bottom:1em; }\nh1{ font-size:24px; }\nh2{ font-size:20px; }\nh3{ font-size:18px; }\nh4{ font-size:16px; }\nh5{ font-size:14px; }\nh6{ font-size:12px; }\np,ul,ol,blockquote,dl,table{ margin:1.2em 0; }\nul,ol{ margin-left:2em; }\nul{ list-style:disc; }\nol{ list-style:decimal; }\nli,li p{ margin:10px 0;}\nimg{ max-width:100%;display:block;margin:0 auto 1em; }\nblockquote{ color:#B5B2B1; border-left:3px solid #aaa; padding:1em; }\nstrong,b{font-weight:bold;}\nem,i{font-style:italic;}\ntable{ width:100%;border-collapse:collapse;border-spacing:1px;margin:1em 0;font-size:.9em; }\nth,td{ padding:5px;text-align:left;border:1px solid #aaa; }\nth{ font-weight:bold;background:#5d5d5d; }\n.symbol-link{font-weight:bold;}\n/* header{ border-bottom:1px solid #494756; } */\n.title{ margin:0 0 8px;line-height:1.3;color:#ddd; }\n.meta {color:#5e5c6d;font-size:13px;margin:0 0 .5em; }\na{text-decoration:none; color:#2a4b87;}\n.meta .head { display: inline-block; overflow: hidden}\n.head .h-thumb { width: 30px; height: 30px; margin: 0; padding: 0; border-radius: 50%; float: left;}\n.head .h-content { margin: 0; padding: 0 0 0 9px; float: left;}\n.head .h-name {font-size: 13px; color: #eee; margin: 0;}\n.head .h-time {font-size: 11px; color: #7E829C; margin: 0;line-height: 11px;}\n.small {font-size: 12.5px; display: inline-block; transform: scale(0.9); -webkit-transform: scale(0.9); transform-origin: left; -webkit-transform-origin: left;}\n.smaller {font-size: 12.5px; display: inline-block; transform: scale(0.8); -webkit-transform: scale(0.8); transform-origin: left; -webkit-transform-origin: left;}\n.bt-text {font-size: 12px;margin: 1.5em 0 0 0}\n.bt-text p {margin: 0}\n</style>\n</head>\n<body>\n<div class=\"wrapper\">\n<header>\n<h2 class=\"title\">\nAugust is among the worst months of year for the stock market. Here's how to play it.\n</h2>\n\n<h4 class=\"meta\">\n\n\n<div class=\"head\" \">\n\n\n<div class=\"h-thumb\" style=\"background-image:url(https://static.tigerbbs.com/150f88aa4d182df19190059f4a365e99);background-size:cover;\"></div>\n\n<div class=\"h-content\">\n<p class=\"h-name\">Dow Jones </p>\n<p class=\"h-time\">2021-08-03 17:45</p>\n</div>\n\n</div>\n\n\n</h4>\n\n</header>\n<article>\n<p>On Wall Street, August is off to a solid start, but the month tends to accompany a bout of turbulence in equity markets.</p>\n<p>The month is associated with the worst performances for the Dow Jones Industrial Average , S&amp;P 500 index , as well as the small cap Russell 2000 and large-cap Russell1000 indexes, over the past three decades, according to the folks at Stock Trader's Almanac.</p>\n<p>The research outfit said that from 1988 to 2020 average declines for the benchmarks ranged from 0.4% for the Russell 2000 to 0.8% by Dow. For the Nasdaq Composite, meanwhile, August ranks as second-worst, with an average gain of 0.2% over the same period, with September being the worst month for the technology-heavy index.</p>\n<p>To be sure, a year ago, in the midst of the COVID-19 pandemic, August produced stellar returns across the board as investors bet on an eventual rebound in pandemic-plagued markets.</p>\n<p>However, last year's uncharacteristically strong performance, which saw monthly gains of over 9% for the Nasdaq Composite and over 7% for the Dow and S&amp;P 500, doesn't mean the long-term trend has changed.</p>\n<p>\"As shown in the LPL Chart of the Day, August and September have been historically two of the weakest months of the year,\" wrote Ryan Detrick, chief market strategist for LPL Financial, in a Monday research note.</p>\n<p>Check out the monthly returns on average since 1950:</p>\n<p>Here are the historical rankings by month via LPL:</p>\n<p>The folks at Bespoke Investment Group put a finer point on the underperformance for August, especially after a strong year-to-date performance, as has been enjoyed in 2021.</p>\n<p>\"Since 1983, the weakest August returns tend to come in years where the S&amp;P 500 was up over 10% YTD heading into the month,\" the researchers note.</p>\n<p>The markets performance thus far has come on the back of stellar earnings results as American corporations rebound from COVID-19, but there are lingering fears that the U.S. has reached or is near peak earnings and economic growth .</p>\n<p><b>So how to play the turbulent stretch?</b></p>\n<p>Jeff Hirsch, editor of the Stock Trader's Almanac, said that the first nine trading days of August tend to be the most prone to weakness while the rest of the month is better. That said, he warns that the expirations of futures and options contracts toward the end of the month tend to create a fresh bout of chop in August, heading toward September, another rough patch for stocks.</p>\n<p>\"The end of August tends to be weaker when traders evacuate Wall Street for the summer finale,\" Hirsch wrote.</p>\n<p>\"Expiration week is down more than half the time since 1990, with some sizable losses,\" he said.</p>\n<p>Stock Trader's Almanac indicated that bullishness prevails in the market, however. \"Bullish forces continue to persist. The Fed remains easy and accommodative. More fiscal stimulus is likely from Washington as Congress nears finalizing the deals on infrastructure and spending,\" the data company wrote. But it cautioned that outperforming second-quarter earnings and the spread of the Delta variant of COVID-19 \"is a concern and poses a threat to the bull and the economic expansion.\"</p>\n<p>\"Political wrangling here in the States and geopolitical machinations around world could also knock the market off course momentarily,\" Stock Trader's Almanac wrote, while noting that its outlook for the S&amp;P 500 sees a push to the 4500-4600 range or even higher.</p>\n<p>Strategists continue to recommend investment prudence, especially with the benchmark 10-year Treasury yields hanging around a multi-month low near 1.15%.</p>\n<p>Bespoke Investment Group also points to a strong 2021, even if the next two months are a bit bumpy, noting that that final stretch of the year tends to be strong when the months leading up to August also have been healthy.</p>\n<p>\"While the average and median returns for August may be lackluster, the final four months of the year have seen an average gain of 5.94% (median: 8.03%) with gains 12 out of 14 times (85%). That's pretty consistent,\" the analysts wrote.</p>\n\n</article>\n</div>\n</body>\n</html>\n","type":0,"thumbnail":"","relate_stocks":{"161125":"标普500","513500":"标普500ETF","OEF":"标普100指数ETF-iShares",".SPX":"S&P 500 Index","IVV":"标普500指数ETF","OEX":"标普100","SPXU":"三倍做空标普500ETF","SDS":"两倍做空标普500ETF","UPRO":"三倍做多标普500ETF","SSO":"两倍做多标普500ETF","SH":"标普500反向ETF"},"is_english":true,"share_image_url":"https://static.laohu8.com/e9f99090a1c2ed51c021029395664489","article_id":"2156100119","content_text":"On Wall Street, August is off to a solid start, but the month tends to accompany a bout of turbulence in equity markets.\nThe month is associated with the worst performances for the Dow Jones Industrial Average , S&P 500 index , as well as the small cap Russell 2000 and large-cap Russell1000 indexes, over the past three decades, according to the folks at Stock Trader's Almanac.\nThe research outfit said that from 1988 to 2020 average declines for the benchmarks ranged from 0.4% for the Russell 2000 to 0.8% by Dow. For the Nasdaq Composite, meanwhile, August ranks as second-worst, with an average gain of 0.2% over the same period, with September being the worst month for the technology-heavy index.\nTo be sure, a year ago, in the midst of the COVID-19 pandemic, August produced stellar returns across the board as investors bet on an eventual rebound in pandemic-plagued markets.\nHowever, last year's uncharacteristically strong performance, which saw monthly gains of over 9% for the Nasdaq Composite and over 7% for the Dow and S&P 500, doesn't mean the long-term trend has changed.\n\"As shown in the LPL Chart of the Day, August and September have been historically two of the weakest months of the year,\" wrote Ryan Detrick, chief market strategist for LPL Financial, in a Monday research note.\nCheck out the monthly returns on average since 1950:\nHere are the historical rankings by month via LPL:\nThe folks at Bespoke Investment Group put a finer point on the underperformance for August, especially after a strong year-to-date performance, as has been enjoyed in 2021.\n\"Since 1983, the weakest August returns tend to come in years where the S&P 500 was up over 10% YTD heading into the month,\" the researchers note.\nThe markets performance thus far has come on the back of stellar earnings results as American corporations rebound from COVID-19, but there are lingering fears that the U.S. has reached or is near peak earnings and economic growth .\nSo how to play the turbulent stretch?\nJeff Hirsch, editor of the Stock Trader's Almanac, said that the first nine trading days of August tend to be the most prone to weakness while the rest of the month is better. That said, he warns that the expirations of futures and options contracts toward the end of the month tend to create a fresh bout of chop in August, heading toward September, another rough patch for stocks.\n\"The end of August tends to be weaker when traders evacuate Wall Street for the summer finale,\" Hirsch wrote.\n\"Expiration week is down more than half the time since 1990, with some sizable losses,\" he said.\nStock Trader's Almanac indicated that bullishness prevails in the market, however. \"Bullish forces continue to persist. The Fed remains easy and accommodative. More fiscal stimulus is likely from Washington as Congress nears finalizing the deals on infrastructure and spending,\" the data company wrote. But it cautioned that outperforming second-quarter earnings and the spread of the Delta variant of COVID-19 \"is a concern and poses a threat to the bull and the economic expansion.\"\n\"Political wrangling here in the States and geopolitical machinations around world could also knock the market off course momentarily,\" Stock Trader's Almanac wrote, while noting that its outlook for the S&P 500 sees a push to the 4500-4600 range or even higher.\nStrategists continue to recommend investment prudence, especially with the benchmark 10-year Treasury yields hanging around a multi-month low near 1.15%.\nBespoke Investment Group also points to a strong 2021, even if the next two months are a bit bumpy, noting that that final stretch of the year tends to be strong when the months leading up to August also have been healthy.\n\"While the average and median returns for August may be lackluster, the final four months of the year have seen an average gain of 5.94% (median: 8.03%) with gains 12 out of 14 times (85%). That's pretty consistent,\" the analysts wrote.","news_type":1},"isVote":1,"tweetType":1,"viewCount":857,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"EN","totalScore":0},{"id":804772539,"gmtCreate":1627984888021,"gmtModify":1703499096140,"author":{"id":"3577522329316309","authorId":"3577522329316309","name":"pompeepee","avatar":"https://static.laohu8.com/default-avatar.jpg","crmLevel":2,"crmLevelSwitch":0,"followedFlag":false,"idStr":"3577522329316309","authorIdStr":"3577522329316309"},"themes":[],"htmlText":"wah","listText":"wah","text":"wah","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":5,"commentSize":0,"repostSize":0,"link":"https://ttm.financial/post/804772539","repostId":"2156100119","repostType":4,"isVote":1,"tweetType":1,"viewCount":483,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"EN","totalScore":0},{"id":805580995,"gmtCreate":1627891862817,"gmtModify":1703497297941,"author":{"id":"3577522329316309","authorId":"3577522329316309","name":"pompeepee","avatar":"https://static.laohu8.com/default-avatar.jpg","crmLevel":2,"crmLevelSwitch":0,"followedFlag":false,"idStr":"3577522329316309","authorIdStr":"3577522329316309"},"themes":[],"htmlText":"wowew","listText":"wowew","text":"wowew","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":1,"commentSize":1,"repostSize":0,"link":"https://ttm.financial/post/805580995","repostId":"1188442648","repostType":4,"repost":{"id":"1188442648","kind":"news","pubTimestamp":1627890543,"share":"https://ttm.financial/m/news/1188442648?lang=&edition=fundamental","pubTime":"2021-08-02 15:49","market":"other","language":"en","title":"Commodities Week Ahead: Oil, Gold Eye U.S. Jobs Report As China PMI Slides","url":"https://stock-news.laohu8.com/highlight/detail?id=1188442648","media":"investing.com","summary":"It’s that time again. The release of the monthly US jobs report. And the direction of gold, oil and ","content":"<p>It’s that time again. The release of the monthly&nbsp;US jobs report. And the direction of&nbsp;gold,&nbsp;oil&nbsp;and a few other key commodities could well depend on how healthy the labor market in the world’s leading economy is.</p>\n<p>It can be argued that every US jobs report holds markets hostage 'til its release.</p>\n<p>But this report for July might be unusually important for three reasons: One, it will show how well America is hiring amid suspicion that government aid for the unemployed is keeping many from getting jobs; two, it will be a referendum on the US economy amid the resurgence of COVID cases from the Delta variant of the virus; and three, it will also demonstrate if the United States will assure the world of growth just as China’s economy was slacking.</p>\n<p>China's&nbsp;factory data, released on Monday, showed activity expanded in July at the slowest pace in 17 months as higher raw material costs, equipment maintenance and extreme weather weighed on business activity.&nbsp; The data added to concerns about a slowdown in the world's second-biggest economy.</p>\n<p><img src=\"https://static.tigerbbs.com/7e4e598a6558955419506b0cfefc5975\" tg-width=\"816\" tg-height=\"744\" referrerpolicy=\"no-referrer\" width=\"100%\" height=\"auto\">Oil Weekly TTM</p>\n<p>Edward Moya, senior analyst at OANDA, said oil prices, particularly, were sensitive to talk of any China slowdown, adding:</p>\n<blockquote>\n \"China's been leading economic recovery in Asia and if the pullback deepens, concerns will grow that the global outlook will see a significant decline.\"The crude demand outlook is on shaky ground and that probably will not improve until global vaccinations improve.\"\n</blockquote>\n<p>New York-traded West Texas Intermediate crude and London’s&nbsp;Brentwere both down about 1% each in Monday’s afternoon trade in Asia, after posting modest gains for July, making it oil’s positive run to a fourth straight month.</p>\n<p>Also weighing on oil was a Reuters survey that found production from the Organization of the Petroleum Exporting Countries hitting 16 month highs last month as the group further eased production curbs under a pact with its allies and top exporter Saudi Arabia.</p>\n<p>While coronavirus cases continue to climb globally, analysts said higher vaccination rates would limit the need for the harsh lockdowns that gutted demand during the peak of the pandemic last year. The United States will not lock down again to curb COVID-19 but \"things are going to get worse\" as the Delta variant fuels a surge in cases, mostly among the unvaccinated, top US infectious disease expert Anthony Fauci said Sunday.</p>\n<p>Hence, the importance of the July nonfarm payrolls report due Friday.</p>\n<p>Economists are expecting the economy to have added 900,000 jobs in July after a forecast-beating 850,000 in June.</p>\n<p>Last week Fed Chair Jerome Powell said the job market still had \"some ground to cover\" before it would be time to start scaling back stimulus measures the central bank enacted in the spring of 2020 to combat the economic fallout from the coronavirus pandemic.</p>\n<p>In June Fed officials began debating how to wind down bond purchases, but there is no clear timetable yet for when it will begin pulling back emergency market support measures.</p>\n<p><b>Treacherous Waters For Gold If Jobs Numbers Surprise</b></p>\n<p>Oil aside, gold and&nbsp;copper&nbsp;will also likely be heavily influenced by the July payrolls report.</p>\n<p>After two weeks of anemic action, gold longs got a break last week when Federal Reserve Chair Jerome Powell said the central bank wasn’t ready to raise US interest rates as it was still focused on buying assets to support an economy recovering from the coronavirus pandemic.</p>\n<p>Powell also refused to discuss when the Fed might consider tapering the combined $120 billion it was plonking down each month into Treasury bonds and agency mortgage‑backed securities. His mantra: It wasn’t time for that.</p>\n<p><img src=\"https://static.tigerbbs.com/3ef5b83aa16320d74287cd6de18a59bd\" tg-width=\"853\" tg-height=\"746\" referrerpolicy=\"no-referrer\" width=\"100%\" height=\"auto\">Gold Weekly TTM</p>\n<p>Front-month gold on New York’s Comex was down 0.2% in Monday’s afternoon trade in Asia, hovering at under $1,815 an ounce.</p>\n<p>If gold clears $1,850, it might be able to make a run toward $1,900, analysts say.</p>\n<p>The risk, however, is US jobs showing a bigger-than-expected gain for July in the Labor Department’s monthly nonfarm payroll report due at the end of this week. If that overshoots forecasts, it could complicate the Fed’s aim of keeping the stimulus on for the foreseeable future and rates lower for longer. Gold might be caught in treacherous waters again if the job numbers surprise.</p>\n<p>Aside from the jobs report, the economic calendar also features other important data including the Institute for Supply Management’s&nbsp;manufacturing&nbsp;data Monday and&nbsp;service sector&nbsp;data on Wednesday. The ISM manufacturing PMI is expected to remain robust, but to again underline supply side strains in the economy that are contributing to higherinflation.</p>\n<p>Data on&nbsp;factory orders&nbsp;is slated for Tuesday and the weekly report oninitial jobless claimsis on Thursday. Jobless claims have fallen considerably since the start of the year amid growing labor demand, but the Delta variant that’s fueled a recent surge in new infections across the country poses a risk.</p>\n<p>Several Fed officials are also scheduled to speak during the week, including Boston Fed President Eric Rosengren, Fed Vice Chair&nbsp;Richard Clarida&nbsp;and Fed Governor&nbsp;Christopher Waller.</p>","source":"lsy1594375853987","collect":0,"html":"<!DOCTYPE html>\n<html>\n<head>\n<meta http-equiv=\"Content-Type\" content=\"text/html; charset=utf-8\" />\n<meta name=\"viewport\" content=\"width=device-width,initial-scale=1.0,minimum-scale=1.0,maximum-scale=1.0,user-scalable=no\"/>\n<meta name=\"format-detection\" content=\"telephone=no,email=no,address=no\" />\n<title>Commodities Week Ahead: Oil, Gold Eye U.S. Jobs Report As China PMI Slides</title>\n<style type=\"text/css\">\na,abbr,acronym,address,applet,article,aside,audio,b,big,blockquote,body,canvas,caption,center,cite,code,dd,del,details,dfn,div,dl,dt,\nem,embed,fieldset,figcaption,figure,footer,form,h1,h2,h3,h4,h5,h6,header,hgroup,html,i,iframe,img,ins,kbd,label,legend,li,mark,menu,nav,\nobject,ol,output,p,pre,q,ruby,s,samp,section,small,span,strike,strong,sub,summary,sup,table,tbody,td,tfoot,th,thead,time,tr,tt,u,ul,var,video{ font:inherit;margin:0;padding:0;vertical-align:baseline;border:0 }\nbody{ font-size:16px; line-height:1.5; color:#999; background:transparent; }\n.wrapper{ overflow:hidden;word-break:break-all;padding:10px; }\nh1,h2{ font-weight:normal; line-height:1.35; margin-bottom:.6em; }\nh3,h4,h5,h6{ line-height:1.35; margin-bottom:1em; }\nh1{ font-size:24px; }\nh2{ font-size:20px; }\nh3{ font-size:18px; }\nh4{ font-size:16px; }\nh5{ font-size:14px; }\nh6{ font-size:12px; }\np,ul,ol,blockquote,dl,table{ margin:1.2em 0; }\nul,ol{ margin-left:2em; }\nul{ list-style:disc; }\nol{ list-style:decimal; }\nli,li p{ margin:10px 0;}\nimg{ max-width:100%;display:block;margin:0 auto 1em; }\nblockquote{ color:#B5B2B1; border-left:3px solid #aaa; padding:1em; }\nstrong,b{font-weight:bold;}\nem,i{font-style:italic;}\ntable{ width:100%;border-collapse:collapse;border-spacing:1px;margin:1em 0;font-size:.9em; }\nth,td{ padding:5px;text-align:left;border:1px solid #aaa; }\nth{ font-weight:bold;background:#5d5d5d; }\n.symbol-link{font-weight:bold;}\n/* header{ border-bottom:1px solid #494756; } */\n.title{ margin:0 0 8px;line-height:1.3;color:#ddd; }\n.meta {color:#5e5c6d;font-size:13px;margin:0 0 .5em; }\na{text-decoration:none; color:#2a4b87;}\n.meta .head { display: inline-block; overflow: hidden}\n.head .h-thumb { width: 30px; height: 30px; margin: 0; padding: 0; border-radius: 50%; float: left;}\n.head .h-content { margin: 0; padding: 0 0 0 9px; float: left;}\n.head .h-name {font-size: 13px; color: #eee; margin: 0;}\n.head .h-time {font-size: 11px; color: #7E829C; margin: 0;line-height: 11px;}\n.small {font-size: 12.5px; display: inline-block; transform: scale(0.9); -webkit-transform: scale(0.9); transform-origin: left; -webkit-transform-origin: left;}\n.smaller {font-size: 12.5px; display: inline-block; transform: scale(0.8); -webkit-transform: scale(0.8); transform-origin: left; -webkit-transform-origin: left;}\n.bt-text {font-size: 12px;margin: 1.5em 0 0 0}\n.bt-text p {margin: 0}\n</style>\n</head>\n<body>\n<div class=\"wrapper\">\n<header>\n<h2 class=\"title\">\nCommodities Week Ahead: Oil, Gold Eye U.S. Jobs Report As China PMI Slides\n</h2>\n\n<h4 class=\"meta\">\n\n\n2021-08-02 15:49 GMT+8&nbsp;&nbsp;&nbsp;<a href=https://www.investing.com/analysis/commodities-week-ahead-oil-gold-eye-us-jobs-report-as-china-pmi-slides-200595381><strong>investing.com</strong></a>\n\n\n</h4>\n\n</header>\n<article>\n<div>\n<p>It’s that time again. The release of the monthly US jobs report. And the direction of gold, oil and a few other key commodities could well depend on how healthy the labor market in the world’s leading...</p>\n\n<a href=\"https://www.investing.com/analysis/commodities-week-ahead-oil-gold-eye-us-jobs-report-as-china-pmi-slides-200595381\">Web Link</a>\n\n</div>\n\n\n</article>\n</div>\n</body>\n</html>\n","type":0,"thumbnail":"","relate_stocks":{},"source_url":"https://www.investing.com/analysis/commodities-week-ahead-oil-gold-eye-us-jobs-report-as-china-pmi-slides-200595381","is_english":true,"share_image_url":"https://static.laohu8.com/e9f99090a1c2ed51c021029395664489","article_id":"1188442648","content_text":"It’s that time again. The release of the monthly US jobs report. And the direction of gold, oil and a few other key commodities could well depend on how healthy the labor market in the world’s leading economy is.\nIt can be argued that every US jobs report holds markets hostage 'til its release.\nBut this report for July might be unusually important for three reasons: One, it will show how well America is hiring amid suspicion that government aid for the unemployed is keeping many from getting jobs; two, it will be a referendum on the US economy amid the resurgence of COVID cases from the Delta variant of the virus; and three, it will also demonstrate if the United States will assure the world of growth just as China’s economy was slacking.\nChina's factory data, released on Monday, showed activity expanded in July at the slowest pace in 17 months as higher raw material costs, equipment maintenance and extreme weather weighed on business activity.  The data added to concerns about a slowdown in the world's second-biggest economy.\nOil Weekly TTM\nEdward Moya, senior analyst at OANDA, said oil prices, particularly, were sensitive to talk of any China slowdown, adding:\n\n \"China's been leading economic recovery in Asia and if the pullback deepens, concerns will grow that the global outlook will see a significant decline.\"The crude demand outlook is on shaky ground and that probably will not improve until global vaccinations improve.\"\n\nNew York-traded West Texas Intermediate crude and London’s Brentwere both down about 1% each in Monday’s afternoon trade in Asia, after posting modest gains for July, making it oil’s positive run to a fourth straight month.\nAlso weighing on oil was a Reuters survey that found production from the Organization of the Petroleum Exporting Countries hitting 16 month highs last month as the group further eased production curbs under a pact with its allies and top exporter Saudi Arabia.\nWhile coronavirus cases continue to climb globally, analysts said higher vaccination rates would limit the need for the harsh lockdowns that gutted demand during the peak of the pandemic last year. The United States will not lock down again to curb COVID-19 but \"things are going to get worse\" as the Delta variant fuels a surge in cases, mostly among the unvaccinated, top US infectious disease expert Anthony Fauci said Sunday.\nHence, the importance of the July nonfarm payrolls report due Friday.\nEconomists are expecting the economy to have added 900,000 jobs in July after a forecast-beating 850,000 in June.\nLast week Fed Chair Jerome Powell said the job market still had \"some ground to cover\" before it would be time to start scaling back stimulus measures the central bank enacted in the spring of 2020 to combat the economic fallout from the coronavirus pandemic.\nIn June Fed officials began debating how to wind down bond purchases, but there is no clear timetable yet for when it will begin pulling back emergency market support measures.\nTreacherous Waters For Gold If Jobs Numbers Surprise\nOil aside, gold and copper will also likely be heavily influenced by the July payrolls report.\nAfter two weeks of anemic action, gold longs got a break last week when Federal Reserve Chair Jerome Powell said the central bank wasn’t ready to raise US interest rates as it was still focused on buying assets to support an economy recovering from the coronavirus pandemic.\nPowell also refused to discuss when the Fed might consider tapering the combined $120 billion it was plonking down each month into Treasury bonds and agency mortgage‑backed securities. His mantra: It wasn’t time for that.\nGold Weekly TTM\nFront-month gold on New York’s Comex was down 0.2% in Monday’s afternoon trade in Asia, hovering at under $1,815 an ounce.\nIf gold clears $1,850, it might be able to make a run toward $1,900, analysts say.\nThe risk, however, is US jobs showing a bigger-than-expected gain for July in the Labor Department’s monthly nonfarm payroll report due at the end of this week. If that overshoots forecasts, it could complicate the Fed’s aim of keeping the stimulus on for the foreseeable future and rates lower for longer. Gold might be caught in treacherous waters again if the job numbers surprise.\nAside from the jobs report, the economic calendar also features other important data including the Institute for Supply Management’s manufacturing data Monday and service sector data on Wednesday. The ISM manufacturing PMI is expected to remain robust, but to again underline supply side strains in the economy that are contributing to higherinflation.\nData on factory orders is slated for Tuesday and the weekly report oninitial jobless claimsis on Thursday. Jobless claims have fallen considerably since the start of the year amid growing labor demand, but the Delta variant that’s fueled a recent surge in new infections across the country poses a risk.\nSeveral Fed officials are also scheduled to speak during the week, including Boston Fed President Eric Rosengren, Fed Vice Chair Richard Clarida and Fed Governor Christopher Waller.","news_type":1},"isVote":1,"tweetType":1,"viewCount":492,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"EN","totalScore":0}],"defaultTab":"following","isTTM":true}