Daiichi Sankyo Co., Ltd.(DSKYF),Stock Price, Discussion, News, Quote & History - To The Moon - Tiger Brokers Online Investing Community

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DSKYF Daiichi Sankyo Co., Ltd.

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{"stockData":{"symbol":"DSKYF","market":"US","secType":"STK","nameCN":"Daiichi Sankyo Co., Ltd.","latestPrice":22.65,"timestamp":1743192000000,"preClose":24,"halted":0,"volume":10918,"delay":15,"floatShares":1876450459,"shares":1916602000,"eps":0.742527,"marketStatus":"Market Closed","change":-1.35,"latestTime":"03-28 16:00:00 EDT Delay","open":22.81,"high":25.89,"low":22.65,"amount":262892.27,"amplitude":0.135,"askPrice":0,"askSize":0,"bidPrice":0,"bidSize":0,"shortable":3,"etf":0,"otc":true,"ttmEps":0.742527,"tradingStatus":0,"nextMarketStatus":{"tag":"Pre-Market Trading","tradingStatus":1,"beginTime":1743408000000},"marketStatusCode":7,"adr":0,"adrRate":0,"exchange":"PINK LIMITED","adjPreClose":24,"volumeRatio":0.9281014559232437},"requestUrl":"/m/hq/s/DSKYF","defaultTab":"news","newsList":[{"id":"2519880380","title":"TAK or DSNKY: Which Is the Better Value Stock Right Now?","url":"https://stock-news.laohu8.com/highlight/detail?id=2519880380","media":"Zacks","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2519880380?lang=en_us&edition=full_marsco","pubTime":"2025-03-14 23:40","pubTimestamp":1741966808,"startTime":"0","endTime":"0","summary":"Investors interested in Medical - Drugs stocks are likely familiar with Takeda Pharmaceutical Co.  and Daiichi Sankyo Co., Ltd. - Sponsored ADR . But which of these two stocks is more attractive to value investors?We'll need to take a closer look to find out.There are plenty of strategies for discovering value stocks, but we have found that pairing a strong Zacks Rank with an impressive grade in the Value category of our Style Scores system produces the best returns. The proven Zacks Rank puts an emphasis on earnings estimates and estimate revisions, while our Style Scores work to identify stocks with specific traits.Currently, Takeda Pharmaceutical Co. has a Zacks Rank of #2 , while Daiichi Sankyo Co., Ltd. - Sponsored ADR has a Zacks Rank of #3 . Investors should feel comfortable knowing that TAK likely has seen a stronger improvement to its earnings outlook than DSNKY has recently. However, value investors will care about much more than just this.This article originally published on","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/tak-dsnky-better-value-stock-154008572.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["BK4007","DSKYF","TAK","DSNKY"],"gpt_icon":0},{"id":"2517445082","title":"J.P. Morgan Remains a Buy on Daiichi Sankyo Company (DSKYF)","url":"https://stock-news.laohu8.com/highlight/detail?id=2517445082","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2517445082?lang=en_us&edition=full_marsco","pubTime":"2025-03-08 20:07","pubTimestamp":1741435630,"startTime":"0","endTime":"0","summary":"J.P. Morgan analyst Seiji Wakao maintained a Buy rating on Daiichi Sankyo Company (DSKYF – Research Report) on March 5 and set a price target of Ye...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/blurbs/j-p-morgan-remains-a-buy-on-daiichi-sankyo-company-dskyf?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/blurbs/j-p-morgan-remains-a-buy-on-daiichi-sankyo-company-dskyf?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["LU0795875169.SGD","LU2089283258.USD","LU1732799900.SGD","LU1668664300.SGD","LU1548497426.USD","BK4127","IE00BZ1G4Q59.USD","LU1732800096.USD","LU1989772840.SGD","LU2111349929.HKD","LU0267386448.USD","LU2089284900.SGD","DSKYF","LU1162221912.USD","LU1720051017.SGD","LU1074936037.SGD","LU0225283273.USD","BK4504","LU0158827948.USD","LU0106831901.USD","BK4516","BK4585","LU0795875086.SGD","LU2357305700.SGD","LU0320765646.SGD","LU0098860793.USD","LU0912757837.SGD","LU1989772923.USD","BK4588","LU0006306889.USD","BK4007","IE00BKVL7J92.USD","LU0106261372.USD","LU0158827781.USD","BK4581","LU2023251221.USD","LU0314104364.USD","LU1363072403.SGD","LU2271345857.HKD","LU2347655156.SGD","LU2133065610.SGD","LU1720051108.HKD","LU2028103732.USD","BK4534","LU0971096721.USD"],"gpt_icon":0},{"id":"2516920633","title":"ENHERTU® Demonstrated Statistically Significant and Clinically Meaningful Improvement in Overall Survival in Patients with HER2 Positive Metastatic Gastric Cancer at Interim Analysis of DESTINY-Gastric04 Phase 3 Trial","url":"https://stock-news.laohu8.com/highlight/detail?id=2516920633","media":"Business Wire","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2516920633?lang=en_us&edition=full_marsco","pubTime":"2025-03-03 21:00","pubTimestamp":1741006800,"startTime":"0","endTime":"0","summary":"Phase 3 results confirm the efficacy of Daiichi Sankyo and AstraZeneca’s ENHERTU in second-line metastatic gastric cancer. DESTINY-Gastric04 will be unblinded at interim analysis based on the superior efficacy of ENHERTU. TOKYO & BASKING RIDGE, N.J., March 03, 2025----Positive topline results from the DESTINY-Gastric04 phase 3 trial showed ENHERTU  demonstrated a statistically significant and clinically meaningful improvement in the primary endpoint of overall survival  compared to ramucirumab and paclitaxel in patients with second-line HER2 positive  unresectable and/or metastatic gastric or gastroesophageal junction  adenocarcinoma.\"We are committed to advancing the care of patients with metastatic gastric cancer and continuing to understand the role of ENHERTU in earlier lines of treatment,\" said Susan Galbraith, MBBChir, PhD, Executive Vice President, Oncology Hematology R&D, AstraZeneca. \"The results of DESTINY-Gastric04 show that second-line treatment with ENHERTU can extend surv","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/enhertu-demonstrated-statistically-significant-clinically-130000294.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["DSNKY","BK4097","BK4080","PBD","BK4007","BK4231","DSKYF","OS","ADC","HR","BK4225","BK4203"],"gpt_icon":0},{"id":"2514329672","title":"ENHERTU® Recommended for Approval in the EU by CHMP for Patients with HER2 Low or HER2 Ultralow Metastatic Breast Cancer Following at Least One Endocrine Therapy","url":"https://stock-news.laohu8.com/highlight/detail?id=2514329672","media":"Business Wire","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2514329672?lang=en_us&edition=full_marsco","pubTime":"2025-02-28 21:00","pubTimestamp":1740747600,"startTime":"0","endTime":"0","summary":"Recommendation based on DESTINY-Breast06 phase 3 trial results which showed ENHERTU demonstrated superiority versus chemotherapy with a median progression-free survival of more than one year. TOKYO & MUNICH, February 28, 2025----Daiichi Sankyo  and AstraZeneca’s  ENHERTU  has been recommended for approval in the European Union  as a monotherapy for the treatment of adult patients with unresectable or metastatic hormone receptor  positive, HER2 low  or HER2 ultralow  breast cancer who have received at least one endocrine therapy in the metastatic setting and who are not considered suitable for endocrine therapy as the next line of treatment.ENHERTU is a specifically engineered HER2 directed DXd antibody drug conjugate  discovered by Daiichi Sankyo and being jointly developed and commercialized by Daiichi Sankyo and AstraZeneca.In the DESTINY-Breast06 trial, ENHERTU demonstrated a 38% reduction in the risk of disease progression or death versus chemotherapy in patients with chemotherapy-","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/enhertu-recommended-approval-eu-chmp-130000849.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["HR","BK4087","BK4203","BK4225","BK4231","ORR","BK4007","BK4211","BK4156","CHMP","ADC","BK4195","PBD","DSKYF","BK4080","PFS","DSNKY"],"gpt_icon":0},{"id":"2512922084","title":"TAK vs. DSNKY: Which Stock Is the Better Value Option?","url":"https://stock-news.laohu8.com/highlight/detail?id=2512922084","media":"Zacks","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2512922084?lang=en_us&edition=full_marsco","pubTime":"2025-02-18 00:40","pubTimestamp":1739810413,"startTime":"0","endTime":"0","summary":"Investors with an interest in Medical - Drugs stocks have likely encountered both Takeda Pharmaceutical Co.  and Daiichi Sankyo Co., Ltd. - Sponsored ADR . But which of these two stocks is more attractive to value investors?We'll need to take a closer look to find out.We have found that the best way to discover great value opportunities is to pair a strong Zacks Rank with a great grade in the Value category of our Style Scores system. The proven Zacks Rank puts an emphasis on earnings estimates and estimate revisions, while our Style Scores work to identify stocks with specific traits.Takeda Pharmaceutical Co. and Daiichi Sankyo Co., Ltd. - Sponsored ADR are sporting Zacks Ranks of #2  and #3 , respectively, right now. Investors should feel comfortable knowing that TAK likely has seen a stronger improvement to its earnings outlook than DSNKY has recently. However, value investors will care about much more than just this.","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/tak-vs-dsnky-stock-better-164013572.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["BK4007","DSKYF","DSNKY","TAK"],"gpt_icon":0},{"id":"2508481451","title":"Survey Reveals: 88% of Western Europeans Would Like Better Information on Breast Cancer, Misconceptions and Lack of Awareness of the Disease Still Prevail","url":"https://stock-news.laohu8.com/highlight/detail?id=2508481451","media":"Business Wire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2508481451?lang=en_us&edition=full_marsco","pubTime":"2025-02-04 15:00","pubTimestamp":1738652400,"startTime":"0","endTime":"0","summary":"Survey with 7,750 participants highlights the urgent need for more and improved access to information about breast cancer and metastatic breast cancer across Europe. Results emphasise lack of knowledge of breast cancer severity, age of diagnosis and biomarker status. MUNICH & CAMBRIDGE, England, February 04, 2025----A new survey sponsored by Daiichi Sankyo and AstraZeneca reveals that there is a need for more readily available information on breast cancer, with results revealing misconceptions and a lack of public awareness. The survey conducted across the major five European countries with 7,750 respondents found varying levels of public knowledge about breast cancer and metastatic breast cancer*.1. Recognition of challenges in breast cancer: More than one-third of respondents across all countries recognise that breast cancer has not been overcome, especially in Spain (49%) and the UK (46%) where the majority of respondents do not believe in a chance of cure.\"People should not have to","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/survey-reveals-88-western-europeans-070000054.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["WRN","BK4007","ADC","III","BK4080","BK4134","DSKYF","DSNKY","BK4168","BK4231"],"gpt_icon":0},{"id":"2507957937","title":"Datopotamab Deruxtecan Recommended for Approval in the EU by CHMP for Patients with Previously Treated Metastatic HR Positive, HER2 Negative Breast Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2507957937","media":"Business Wire","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2507957937?lang=en_us&edition=full_marsco","pubTime":"2025-01-31 21:00","pubTimestamp":1738328400,"startTime":"0","endTime":"0","summary":"Recommendation based on TROPION-Breast01 results showing Daiichi Sankyo and AstraZeneca’s datopotamab deruxtecan reduced risk of disease progression or death by 37% versus chemotherapy. Datopotamab deruxtecan approved in the U.S. and Japan for same patient population. TOKYO & MUNICH, January 31, 2025----Datopotamab deruxtecan  has been recommended for approval in the European Union  for the treatment of adult patients with unresectable or metastatic hormone receptor  positive, HER2 negative  breast cancer who have received endocrine therapy and at least one line of chemotherapy in the advanced setting.Datopotamab deruxtecan demonstrated a favorable safety profile over chemotherapy with no new safety concerns identified. Grade 3 or higher treatment-related adverse events  occurred in 21% and 45% of patients in the datopotamab deruxtecan and chemotherapy arms, respectively. The most common grade 3 or higher TRAEs were neutropenia , stomatitis , fatigue  and anemia . In the datopotamab de","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/datopotamab-deruxtecan-recommended-approval-eu-130000461.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["BK4203","BK4007","HR","DSKYF","CR","BK4211","ADC","BK4087","ORR","BK4080","BK4156","BK4195","BK4213","PFS","CHMP","BK4161","BK4225","DSNKY","PR","PBD","BK4231"],"gpt_icon":0},{"id":"2507982654","title":"Daiichi Sankyo Appoints Hiroyuki Okuzawa as Chief Executive Officer","url":"https://stock-news.laohu8.com/highlight/detail?id=2507982654","media":"Business Wire","labels":["executive"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2507982654?lang=en_us&edition=full_marsco","pubTime":"2025-01-31 12:05","pubTimestamp":1738296300,"startTime":"0","endTime":"0","summary":"TOKYO, January 31, 2025----Daiichi Sankyo Company, Ltd  has appointed Hiroyuki Okuzawa, 62, to succeed Sunao Manabe, DVM, Ph.D. as Chief Executive Officer , effective April 1, 2025.Dr. Manabe will transition from his current role of Representative Director, Executive Chairperson and CEO to Representative Director and Executive Chairperson while Mr. Okuzawa will transition to Representative Director, President and CEO.Under Dr. Manabe’s leadership, Daiichi Sankyo’s pioneering science and technology led to the resurgence of antibody drug conjugate  development within the pharmaceutical industry, leading to three of the largest licensing deals in history along with the approvals of ENHERTU and DATROWAY, two precision cancer medicines invented with Daiichi Sankyo’s DXd ADC Technology that are changing the way that metastatic breast cancer is treated.\"I am deeply honored to be the next CEO of Daiichi Sankyo and will follow Sunao Manabe’s exceptional leadership and unwavering commitment to p","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/daiichi-sankyo-appoints-hiroyuki-okuzawa-040500175.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"executive","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["BK4198","LU1992135472.HKD","GB00BDT5M118.USD","LU1992135399.USD","LU2272731600.USD","LU2272731782.SGD","ADC","BK4080","BK4585","DSKYF","LU2211815571.USD","BK4231","BK4588","CFO","CEO","COO","DSNKY","BK4007"],"gpt_icon":0},{"id":"2507841229","title":"TROPION-Lung12 Phase 3 Trial Initiated Evaluating DATROWAY® as Part of Adjuvant Regimen for Patients with Early-Stage Non-Small Cell Lung Cancer at High Risk of Relapse","url":"https://stock-news.laohu8.com/highlight/detail?id=2507841229","media":"Business Wire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2507841229?lang=en_us&edition=full_marsco","pubTime":"2025-01-31 12:00","pubTimestamp":1738296000,"startTime":"0","endTime":"0","summary":"TOKYO & BASKING RIDGE, N.J., January 31, 2025----The first patient has been dosed in the TROPION-Lung12 phase 3 trial evaluating the efficacy and safety of adjuvant DATROWAY  plus rilvegostomig or rilvegostomig monotherapy versus standard of care in patients with stage 1 adenocarcinoma non-small cell lung cancer  after complete surgical resection who are ctDNA-positive or have other high risk pathological features.\"With TROPION-Lung12, we are simultaneously deploying a novel strategy for identifying patients with lung cancer who are at an increased risk of disease recurrence after surgery and evaluating novel treatment options in the adjuvant setting, including rilvegostomig with and without DATROWAY,\" said Cristian Massacesi, MD, Chief Medical Officer and Oncology Chief Development Officer, AstraZeneca. \"The ambitious approach in this trial underscores our commitment to both enabling more personalized treatment decisions and delivering innovative treatment options to patients with can","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/tropion-lung12-phase-3-trial-040000069.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["HR","BK4203","DSNKY","BK4231","BK4080","PBD","DSKYF","SSI","BK4007","BK4225","ADC"],"gpt_icon":0},{"id":"2507823687","title":"J.P. Morgan Keeps Their Buy Rating on Daiichi Sankyo Company (DSKYF)","url":"https://stock-news.laohu8.com/highlight/detail?id=2507823687","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2507823687?lang=en_us&edition=full_marsco","pubTime":"2025-01-29 20:08","pubTimestamp":1738152530,"startTime":"0","endTime":"0","summary":"In a report released yesterday, Seiji Wakao from J.P. Morgan maintained a Buy rating on Daiichi Sankyo Company (DSKYF – Research Report), with a pr...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/blurbs/j-p-morgan-keeps-their-buy-rating-on-daiichi-sankyo-company-dskyf?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":["rate","earning"],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/blurbs/j-p-morgan-keeps-their-buy-rating-on-daiichi-sankyo-company-dskyf?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["DSKYF"],"gpt_icon":0},{"id":"2507611549","title":"FDA Expands Label of AZN's Enhertu for New Breast Cancer Indication","url":"https://stock-news.laohu8.com/highlight/detail?id=2507611549","media":"Zacks","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2507611549?lang=en_us&edition=full_marsco","pubTime":"2025-01-29 00:11","pubTimestamp":1738080660,"startTime":"0","endTime":"0","summary":"AstraZenecaAZN and partner Daiichi Sankyo announced that the FDA has approved the supplemental biologics license application  seeking approval for expanded use of Enhertu  for HER2-low metastatic breast cancer in the United States. The approval of the added indication has triggered a $175 million milestone payment from AstraZeneca to Daiichi Sankyo.The companies’ sBLA was seeking approval for Enhertu to treat unresectable or metastatic HR-positive, HER2-low or HER2-ultralow breast cancer in adult patients who have received at least one endocrine therapy in the metastatic setting.The nod in the United States expands the approved indication of Enhertu in HER2-low metastatic breast cancer to include use in an earlier disease setting as well as in a broader patient population that includes HER2-ultralow. The drug has earlier received the FDA’s Breakthrough Therapy designation in the United States for this new indication.In three months, shares of AstraZeneca have lost 6.8% compared with th","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/fda-expands-label-azns-enhertu-161100900.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["BK4548","ALNY","BMRN","LU1829250122.USD","LU0320765992.SGD","LU2417539215.USD","ADC","PFS","DSKYF","LU0889565916.HKD","BK4196","LU2456880835.USD","DSNKY","AZN","BK4566","LU0109394709.USD","BK4139","BK4195","BK4568","LU2236285917.USD","IE00B7SZLL34.SGD","LU2462157665.USD","BK4007","BK4588","CSTL","BK4585","IE0002270589.USD","IE00B19Z3581.USD","BK4231","BK4211","BK4080","IE00B19Z3B42.SGD"],"gpt_icon":0},{"id":"2506375776","title":"Bernstein Reaffirms Their Buy Rating on Daiichi Sankyo Company (DSKYF)","url":"https://stock-news.laohu8.com/highlight/detail?id=2506375776","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2506375776?lang=en_us&edition=full_marsco","pubTime":"2025-01-27 19:58","pubTimestamp":1737979112,"startTime":"0","endTime":"0","summary":"Bernstein analyst Miki Sogi maintained a Buy rating on Daiichi Sankyo Company (DSKYF – Research Report) today and set a price target of Yen6,400.00...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/blurbs/bernstein-reaffirms-their-buy-rating-on-daiichi-sankyo-company-dskyf-2?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":["rate"],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/blurbs/bernstein-reaffirms-their-buy-rating-on-daiichi-sankyo-company-dskyf-2?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["DSKYF"],"gpt_icon":0},{"id":"2505693202","title":"FDA Approves AstraZeneca's Datroway For Pretreated Breast Cancer Patients","url":"https://stock-news.laohu8.com/highlight/detail?id=2505693202","media":"Benzinga","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2505693202?lang=en_us&edition=full_marsco","pubTime":"2025-01-22 01:54","pubTimestamp":1737482080,"startTime":"0","endTime":"0","summary":"On Friday, the U.S. Food and Drug Administration  approved AstraZeneca Plc’s  Datroway for adult patients with unresectable or metastatic hormone receptor -positive, HER2-negative  breast cancer who have received prior endocrine-based therapy and chemotherapy for unresectable or metastatic disease.The approval was based on results from theTROPION-Breast01Phase 3 trial.Read Next: AstraZeneca Aims to Restore Trust With New Leadership in China Amid Scandal and Sales Decline. The safety profile ofDatrowaywas consistent with the known profile of this medicine, with no new safety concerns identified.In theDatrowayarm, the interstitial lung disease  rate was 4.2% and the majority of events were low grade.Datrowayis a specifically engineered TROP2-directed antibody drug conjugate  discovered by Daiichi Sankyo  , and being jointly developed and commercialised by AstraZeneca and Daiichi Sankyo.Price Action: AZN stock is up 2.43% at $68.22 at last check Tuesday.Charles Schwab Delivers Strong Q4: ","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/fda-approves-astrazenecas-datroway-pretreated-175440598.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["LU1829250122.USD","LU0320765992.SGD","LU2417539215.USD","ADC","PFS","DSKYF","LU0889565916.HKD","DSNKY","AZN","LU0109394709.USD","BK4195","BK4568","LU2236285917.USD","LU2462157665.USD","HR","BK4225","BK4007","BK4588","BK4585","BK4203","BK4231","BK4211","BK4080","LU2456880835.USD"],"gpt_icon":1},{"id":"2504731407","title":"Bernstein Remains a Buy on Daiichi Sankyo Company (DSKYF)","url":"https://stock-news.laohu8.com/highlight/detail?id=2504731407","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2504731407?lang=en_us&edition=full_marsco","pubTime":"2025-01-20 21:05","pubTimestamp":1737378351,"startTime":"0","endTime":"0","summary":"In a report released today, Miki Sogi from Bernstein maintained a Buy rating on Daiichi Sankyo Company (DSKYF – Research Report), with a price targ...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/blurbs/bernstein-remains-a-buy-on-daiichi-sankyo-company-dskyf?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/blurbs/bernstein-remains-a-buy-on-daiichi-sankyo-company-dskyf?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["BK4007","DSKYF"],"gpt_icon":0},{"id":"2503582012","title":"Daiichi Sankyo Acquires Intellectual Property Rights for Anti-TA-MUC1 Antibody in DS-3939 from Glycotope GmbH","url":"https://stock-news.laohu8.com/highlight/detail?id=2503582012","media":"Business Wire","labels":["merge"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2503582012?lang=en_us&edition=full_marsco","pubTime":"2025-01-14 00:00","pubTimestamp":1736784000,"startTime":"0","endTime":"0","summary":"TOKYO & BASKING RIDGE, N.J., January 13, 2025----Daiichi Sankyo Company, Ltd  announced today that it will pay Glycotope $132.5 million to acquire intellectual property rights of the anti-tumor-associated mucin-1  antibody, gatipotuzumab. Such payment by Daiichi Sankyo satisfies all potential clinical, regulatory and sales milestone payments, as well as royalties of products that include gatipotuzumab as part of a 2018 licensing agreement between the parties. In 2018, Daiichi Sankyo in-licensed exclusive rights to develop and commercialize gatipotuzumab worldwide as an antibody drug conjugate  from Glycotope.The anti-TA-MUC1 is the antibody contained in DS-3939, an ADC being developed by Daiichi Sankyo. DS-3939 is a specifically engineered potential first-in-class TA-MUC1 directed medicine designed using Daiichi Sankyo’s proprietary DXd ADC technology. DS-3939 is currently being evaluated in a phase 1/2 clinical trial in patients with several types of advanced solid tumors including no","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/daiichi-sankyo-acquires-intellectual-property-160000039.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"merge","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["BK4231","DSKYF","BK4080","DSNKY","BK4007","ADC","PBD"],"gpt_icon":0},{"id":"2503326508","title":"Datopotamab Deruxtecan Granted Priority Review in the U.S. for Patients with Previously Treated Advanced EGFR-Mutated Non-Small Cell Lung Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2503326508","media":"Business Wire","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2503326508?lang=en_us&edition=full_marsco","pubTime":"2025-01-13 15:00","pubTimestamp":1736751600,"startTime":"0","endTime":"0","summary":"Application based on TROPION-Lung05 phase 2 trial and supported by data from TROPION-Lung01 phase 3 and TROPION-PanTumor01 phase 1 trials. TOKYO & BASKING RIDGE, N.J., January 13, 2025----Daiichi Sankyo  and AstraZeneca’s  Biologics License Application  for datopotamab deruxtecan  has been accepted and granted Priority Review in the U.S. for the treatment of adult patients with locally advanced or metastatic epidermal growth factor receptor-mutated  non-small cell lung cancer  who have received prior systemic therapies, including an EGFR-directed therapy.Datopotamab deruxtecan is a specifically engineered TROP2 directed DXd antibody drug conjugate  discovered by Daiichi Sankyo and being jointly developed by Daiichi Sankyo and AstraZeneca.\"Acquired resistance to front-line therapies and, ultimately, disease progression are unfortunate realities for most patients with advanced EGFR-mutated non-small cell lung cancer,\" said Susan Galbraith, MBBChir, PhD, Executive Vice President, Oncology","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/datopotamab-deruxtecan-granted-priority-review-070000802.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["BK4157","ADC","AEIS","IE00B7SZL793.SGD","PFS","BK4080","BK4195","BK4007","DSNKY","OS","BK4231","DSKYF","IE00B66KJ199.SGD","IE00B19Z4B17.USD","BK4097","BK4211","PBD","IE0031619046.USD"],"gpt_icon":0},{"id":"2494186046","title":"AZN, Daiichi Withdraw EU Filing for Dato-DXd in Nonsquamous NSCLC","url":"https://stock-news.laohu8.com/highlight/detail?id=2494186046","media":"Zacks","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2494186046?lang=en_us&edition=full_marsco","pubTime":"2024-12-26 23:19","pubTimestamp":1735226340,"startTime":"0","endTime":"0","summary":"AstraZeneca AZN and its Japanese partner Daiichi Sankyo announced that they have voluntarily withdrawn the marketing authorization application  for their antibody-drug conjugate , datopotamab deruxtecan .The MAA sought approval of Dato-DXd for treating adult patients with locally advanced or metastatic nonsquamous non-small cell lung cancer  based on the TROPION-Lung01 phase III study.The companies decided to withdraw the MAA for Dato-DXd in nonsquamous NSCLC following feedback from the European Medicines Agency’s Committee for Medicinal Products for Human Use.Last month, AZN and Daiichi Sankyo withdrew the biologics license application  seeking approval of Dato-DXd for the same indication in the United States and instead filed a new BLA for previously treated advanced EGFR-mutated NSCLC.Shares of AstraZeneca have decreased 1.6% in the past year against the industry’s increase of 4%.Earlier this month, the FDA granted a Breakthrough Therapy designation to Dato-DXd for previously treate","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/azn-daiichi-withdraw-eu-filing-151900499.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["LU2361044865.SGD","LU0321505439.SGD","LU2023250843.SGD","LU1934455194.USD","LU0320765489.SGD","LU1934455277.USD","IE00BBT3K403.USD","IE00BN8TJ469.HKD","SG9999001440.SGD","SG9999011175.SGD","IE0002141913.USD","LU1291159041.SGD","SG9999014542.SGD","LU0238689110.USD","IE00B1BXHZ80.USD","LU0861579265.USD","LU0208291251.USD","LU1917777945.USD","LU2023250504.SGD","SG9999014575.USD","LU1061106388.HKD","PFE","LU1941712264.USD","ADC","LU1883839398.USD","SG9999014559.SGD","LU0225284248.USD","IE00BLSP4452.SGD","LU0965509010.AUD","LU0170899867.USD","LU0889565916.HKD","LU1066053197.SGD","MRK","BK4550","IE00B4R5TH58.HKD","LU0109394709.USD","LU1023059063.AUD","DSNKY","AZN","SG9999015341.SGD","LU0225771236.USD","LU1066051811.HKD","LU1430594728.SGD","BK4592","DSKYF","MAA","LU1093756325.SGD","IE00B19Z3B42.SGD","SG9999001176.SGD","SG9999014567.USD","LU1974910355.USD"],"gpt_icon":1},{"id":"2493775992","title":"Datopotamab Deruxtecan Application in the EU for Patients with Advanced Nonsquamous Non-Small Cell Lung Cancer Voluntarily Withdrawn","url":"https://stock-news.laohu8.com/highlight/detail?id=2493775992","media":"Business Wire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2493775992?lang=en_us&edition=full_marsco","pubTime":"2024-12-24 15:00","pubTimestamp":1735023600,"startTime":"0","endTime":"0","summary":"TOKYO & MUNICH, December 24, 2024----Daiichi Sankyo  and AstraZeneca  have voluntarily withdrawn the marketing authorization application  in the EU for datopotamab deruxtecan  for the treatment of adult patients with locally advanced or metastatic nonsquamous non-small cell lung cancer  based on the TROPION-Lung01 phase 3 trial.The decision to withdraw the MAA was informed by feedback from the Committee for Medicinal Products for Human Use of the European Medicines Agency . Daiichi Sankyo and AstraZeneca will continue to work to bring datopotamab deruxtecan to patients with lung cancer in the EU who can benefit and are committed to unlocking the potential of this medicine in lung cancer through our robust clinical development program which includes seven pivotal trials in various lung cancer settings.Datopotamab deruxtecan is a specifically engineered TROP2 directed DXd antibody drug conjugate  discovered by Daiichi Sankyo and being jointly developed by Daiichi Sankyo and AstraZeneca.A","market":"us","thumbnail":"https://s.yimg.com/uu/api/res/1.2/sv.qf7zkcH93Ibh2s9cInQ--~B/aD00NzQ7dz00ODA7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/business-wire.com/e6e065d92bcbe7bb3f01287baca7ae27","type":0,"news_type":0,"thumbnails":["https://s.yimg.com/uu/api/res/1.2/sv.qf7zkcH93Ibh2s9cInQ--~B/aD00NzQ7dz00ODA7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/business-wire.com/e6e065d92bcbe7bb3f01287baca7ae27"],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/datopotamab-deruxtecan-application-eu-patients-070000830.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["IE0031619046.USD","OS","BK4007","IE00B66KJ199.SGD","DSKYF","IE00B19Z4B17.USD","PBD","BK4231","HR","BK4080","BK4211","BK4225","DSNKY","IE00B7SZL793.SGD","BK4156","BK4157","BK4203","MAA","BK4585","PFS","BK4195","BK4215","ADC","BK4097","AEIS","BK4588"],"gpt_icon":0},{"id":"2490048967","title":"AZN, Daiichi's ADC Gets FDA Breakthrough Tag for EGFR-Mutated NSCLC","url":"https://stock-news.laohu8.com/highlight/detail?id=2490048967","media":"Zacks","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2490048967?lang=en_us&edition=full_marsco","pubTime":"2024-12-10 22:44","pubTimestamp":1733841840,"startTime":"0","endTime":"0","summary":"AstraZeneca AZN and its Japanese partner Daiichi Sankyo announced that the FDA has granted a Breakthrough Therapy designation  to their antibody-drug conjugate , datopotamab deruxtecan , for a lung cancer indication.The regulatory granted the BTD to Dato-DXd for the treatment of locally advanced or metastatic epidermal growth factor receptor-mutated  non-small cell lung cancer  in adult patients whose disease progressed on or after treatment with an EGFR-tyrosine kinase inhibitor  and platinum-based chemotherapy.The FDA’s BTD for Dato-DXd was based on data from the phase II TROPION-Lung05 study and supported by data from the phase III TROPION-Lung01 study.Based on the same data, last month, AstraZeneca and Daiichi Sankyo submitted a new biologics license application  seeking accelerated approval of Dato-DXd for previously treated advanced EGFR-mutated NSCLC.Daiichi Sankyo has six ADCs in clinical development across multiple types of cancers, being developed utilizing its DXd ADC techno","market":"us","thumbnail":"https://s.yimg.com/uu/api/res/1.2/6pmiwRZRhtc7hxDNA3zxVQ--~B/aD00MDA7dz02MzU7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/zacks.com/ef77d5a5eb4e72e4dd31ccfaf4ca4ccd","type":0,"news_type":0,"thumbnails":["https://s.yimg.com/uu/api/res/1.2/6pmiwRZRhtc7hxDNA3zxVQ--~B/aD00MDA7dz02MzU7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/zacks.com/ef77d5a5eb4e72e4dd31ccfaf4ca4ccd"],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/azn-daiichis-adc-gets-fda-144400961.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["LU1974910355.USD","LU0289739699.SGD","LU2361045086.USD","BK4516","LU1989771016.USD","LU1829250122.USD","LU0265550946.USD","DSKYF","LU0238689110.USD","SG9999015358.SGD","LU0306807586.USD","LU1061106388.HKD","LU1934455277.USD","LU1941712348.USD","IE00BSNM7G36.USD","LU1894683348.USD","MRK","SG9999001176.SGD","SG9999001440.SGD","LU0965509010.AUD","LU0006306889.USD","LU0225284248.USD","LU0321505868.SGD","LU0889565916.HKD","IE00BN8TJ469.HKD","LU2468319806.SGD","LU0122379950.USD","LU1093756168.USD","IE00BLSP4452.SGD","LU0211331839.USD","BK4007","DSNKY","LU0985481810.HKD","LU0456855351.SGD","SG9999014575.USD","PFE","LU2324357040.USD","SG9999014542.SGD","LU2236285917.USD","LU0070302665.USD","LU2023250504.SGD","ADC","IE00B1BXHZ80.USD","LU0208291251.USD","LU1037948897.HKD","BK4080","LU2462157665.USD","BK4559","LU0170899867.USD","LU0058720904.USD","IE00BJT1NW94.SGD","AZN"],"gpt_icon":1},{"id":"2490013035","title":"QuANTUM-Wild Phase 3 Trial of VANFLYTA® Initiated in Patients with Newly Diagnosed FLT3-ITD Negative AML","url":"https://stock-news.laohu8.com/highlight/detail?id=2490013035","media":"Business Wire","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2490013035?lang=en_us&edition=full_marsco","pubTime":"2024-12-10 21:00","pubTimestamp":1733835600,"startTime":"0","endTime":"0","summary":"TOKYO & BASKING RIDGE, N.J., December 10, 2024----The first patient has been dosed in the QuANTUM-Wild phase 3 trial evaluating Daiichi Sankyo’s  VANFLYTA  in combination with standard intensive induction and consolidation chemotherapy followed by single-agent maintenance in adults with newly diagnosed FLT3-ITD negative acute myeloid leukemia .AML is an aggressive blood cancer with a five-year overall survival rate of approximately 32%.1, 2 Targeted therapy with FLT3 inhibitors has improved survival for some patients with FLT3 gene mutations, which most commonly occur as FLT3-ITD.3 However, about 90% of patients with AML overexpress FLT3 regardless of mutational status.1, 4, 5 No FLT3 inhibitors are currently approved for patients without FLT3 mutations.The QuANTUM-Wild trial was initiated based on results of the QUIWI phase 2 trial evaluating VANFLYTA in combination with standard intensive chemotherapy and as subsequent maintenance monotherapy in adult patients with newly diagnosed FL","market":"us","thumbnail":"https://s.yimg.com/uu/api/res/1.2/LZ.q9Iuft1A.dXEKC2_ciw--~B/aD00NzQ7dz00ODA7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/business-wire.com/c5c6b94e76f92e00dc7e43bf597d2784","type":0,"news_type":0,"thumbnails":["https://s.yimg.com/uu/api/res/1.2/LZ.q9Iuft1A.dXEKC2_ciw--~B/aD00NzQ7dz00ODA7YXBwaWQ9eXRhY2h5b24-/https://media.zenfs.com/en/business-wire.com/c5c6b94e76f92e00dc7e43bf597d2784"],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/quantum-wild-phase-3-trial-130000556.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["HSCT","CR","DSNKY","DSKYF","BK4161","BK4007"],"gpt_icon":0}],"profile":{"websiteUrl":"http://www.daiichisankyo.com","stockEarnings":[{"period":"1week","weight":0.0223},{"period":"1month","weight":0.007},{"period":"3month","weight":0.1808},{"period":"6month","weight":0.2956},{"period":"1year","weight":0.4488},{"period":"ytd","weight":0.7362}],"description":"Daiichi Sankyo Company, Limited manufactures, markets, and sells pharmaceutical products worldwide. The company offers Enhertu, a HER2 directed antibody drug conjugate; Turalio, a CSF-1R inhibitor; Vanflyta, a FLT3 inhibitor for the treatment of adult patients with relapsed/refractory FLT3-ITD acute myeloid leukemia; ferric carboxymaltose injection for treating anaemia; and Injectafer for the treatment for iron deficiency anaemia. It also provides olmesartan medoxomil antihypertensive agents; NILEMDO, an oral treatment to help in lowering cholesterol; and Nustendi, a fixed-dose combination tablet of bempedoic acid and ezetimibe for reducing cholesterol. In addition, the company offers Canalia for the treatment of type 2 diabetes mellitus; Emgalty for the treatment of migraine attacks; Pralia for the treatment of anti-osteoporosis/inhibitor of the progression of bone erosion associated with rheumatoid arthritis; Ranmark for the treatment of bone complications caused by bone metastasis from tumors; Tarlige for treating pain; Tenelia for the treatment of Type 2 diabetes mellitus; Venofer for the treatment of iron deficiency anemia; and Vimpat, an anti-epileptic agent. Further, it provides vaccines for influenza, measles/rubella infection, and mumps. The company has a development and commercialization agreement with Merck to jointly develop and commercialize Daiichi Sankyo's DXd antibody drug conjugate (ADC) candidates The company was founded in 1899 and is headquartered in Tokyo, Japan.","exchange":"PINK LIMITED","name":"Daiichi Sankyo Co., Ltd.","nameEN":"Daiichi Sankyo Co., Ltd."},"APP":{"userAgent":"Mozilla/5.0 AppleWebKit/537.36 (KHTML, like Gecko; compatible; ClaudeBot/1.0; +claudebot@anthropic.com)","isDev":false,"isTTM":true,"deviceId":"web-server-community-laohu8-v3","version":"4.32.1","shortVersion":"4.32.1","platform":"web","vendor":"web","appName":"ttm","isIOS":false,"isAndroid":false,"isTiger":false,"isTHS":false,"isWeiXin":false,"isWeiXinMini":false,"isWeiBo":false,"isQQ":false,"isBaiduSwan":false,"isBaiduBox":false,"isDingTalk":false,"isToutiao":false,"isOnePlus":false,"isHuaWei":false,"isXiaomi":false,"isXiaomiWebView":false,"isOppo":false,"isVivo":false,"isSamsung":false,"isMobile":false},"pagemeta":{"title":"Daiichi Sankyo Co., Ltd.(DSKYF),Stock Price, Discussion, News, Quote & History - To The Moon - Tiger Brokers Online Investing Community","description":"Find the latest Daiichi Sankyo Co., Ltd.(DSKYF) stock quote, history, news, and investing ideas from To The Moon - Tiger Brokers Online Investing Community to stay on top of the markets.","keywords":"Daiichi Sankyo Co., Ltd.,DSKYF,Daiichi Sankyo Co., Ltd.股票,Daiichi Sankyo Co., Ltd.股票老虎,Daiichi Sankyo Co., Ltd.股票老虎国际,Daiichi Sankyo Co., Ltd.行情,Daiichi Sankyo Co., Ltd.股票行情,Daiichi Sankyo Co., Ltd.股价,Daiichi Sankyo Co., Ltd.股市,Daiichi Sankyo Co., Ltd.股票价格,Daiichi Sankyo Co., Ltd.股票交易,Daiichi Sankyo Co., Ltd.股票购买,Daiichi Sankyo Co., Ltd.股票实时行情,购买美股,购买港股,港股开户,美股开户,美股交易,港股交易,开通美港股账户,老虎国际行情","social":{"og_title":"Daiichi Sankyo Co., Ltd.(DSKYF),Stock Price, Discussion, News, Quote & History - To The Moon - Tiger Brokers Online Investing Community","og_description":"Find the latest Daiichi Sankyo Co., Ltd.(DSKYF) stock quote, history, news, and investing ideas from To The Moon - Tiger Brokers Online Investing Community to stay on top of the markets.","og_image":"https://community-static.tradeup.com/news/9b6dafd60190235ae8e2c95f52c583a0"}}}

Introduction