WHO and EMA could approve Novavax Covid vaccine next week

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WHO and EMA could approve Novavax Covid vaccine next week

Financial Times 2021-12-17

US drugmaker ‘confident’ as health bodies signal decisions are on the horizon Medical laboratory scientist Aniela Sobel tests serology samples from the Novavax phase 3 clinical trial in Seattle, ...

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·2021-12-17
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}\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\">\nWHO and EMA could approve Novavax Covid vaccine next week\n</h2>\n\n<h4 class=\"meta\">\n\n\n2021-12-17 07:21 GMT+8&nbsp;&nbsp;&nbsp;<a href=https://www.ft.com/content/a938950e-7f97-46d6-a22c-6933c5634842><strong>Financial Times </strong></a>\n\n\n</h4>\n\n</header>\n<article>\n<div>\n<p>US drugmaker ‘confident’ as health bodies signal decisions are on the horizon\nMedical laboratory scientist Aniela Sobel tests serology samples from the Novavax phase 3 clinical trial in Seattle, ...</p>\n\n<a href=\"https://www.ft.com/content/a938950e-7f97-46d6-a22c-6933c5634842\">Source Link</a>\n\n</div>\n\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"NVAX","symbol_name":"诺瓦瓦克斯医药","start_time":0,"source_url":"https://www.ft.com/content/a938950e-7f97-46d6-a22c-6933c5634842","article_id":"1116963836","we_media_id":null,"thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=1116963836","pubTimestamp":1639696910,"sourceInfo":{"source_id":"lsy1580170736413","name":"The Financial Times"},"weMediaInfo":null,"summary":"US drugmaker ‘confident’ as health bodies signal decisions are on the horizon\nMedical laboratory sci","collect":0,"end_time":0,"defaultTopTitle":"ft.com","property":[],"viewcount":null,"language":"en","relate_stocks":{"NVAX":"诺瓦瓦克斯医药"},"translate_title":"世界卫生组织和欧洲药品管理局可能会在下周批准诺瓦瓦克斯Covid疫苗","themeId":null,"isJumpTheme":false,"ttsUrl":null,"symbols_score_info":{"NVAX":0.9},"content_text":"US drugmaker ‘confident’ as health bodies signal decisions are on the horizon\nMedical laboratory scientist Aniela Sobel tests serology samples from the Novavax phase 3 clinical trial in Seattle, Washington © Karen Ducey/Getty\nThe approvals would provide the US drugmaker with a significant boost after months of delays and share price volatility amid manufacturing issues. The Covid-19 vaccine, also known as Nuvaxovid, would be the Maryland-based company’s first marketed product after more than three decades in business.\nA meeting of an EMA panel has been scheduled for Monday, the agency said, adding that it would communicate more details on that day provided there was a conclusion.\nSeparately, the WHO’s expert panel on vaccines met on Thursday to draft recommendations for use of the vaccine, with the WHO saying it would release its position “in the coming days”.\nWHO approval could come once the health body issued its own emergency use listing, or if the EMA gave it a conditional marketing authorisation, people familiar with the matter said.\nThe step would allow deliveries to begin via global vaccine access scheme Covax. Together with the Serum Institute of India, Novavax has a commitment to supply Covax with 1.1bn doses.\nTwo people familiar with both approval processes said there were still some “open questions” on manufacturing, but that the EMA should be able to issue a conditional approval. The open questions include so-called potency assays and drug substance characterisation — in essence, the ability of Novavax to ensure the product is the same everywhere and the same as that used in clinical studies.\nThe people said Novavax had acknowledged these points in meetings and was working to address them.\n“It’s nothing serious. It’s not different from situations we have seen with previous vaccines,” one of the people said, while also cautioning that an approval was not certain.\nNovavax said both approval processes would consider extensive data on manufacturing as well as clinical and pre-clinical data. The company was “confident that the vaccine meets the stringent regulatory quality, safety and efficacy specifications” needed for authorisation by the WHO and the EMA and it looked forward to their decisions.\nThe EMA declined to comment. The WHO said it would release its position “in the coming days”.\nOne of the people added that the EMA was “racing against time” as the vaccine, which would initially only be approved for a primary series or the first two shots for someone who has not been vaccinated, could play “an important role” this winter.\nThe Novavax shot has already been approved in the Philippines and Indonesia and the drugmaker has filed for approval in the UK. The company also expects to submit a complete application to the US Food and Drug Administration by year’s end.\nIn contrast to the novel mRNA vaccines made by Moderna and Pfizer, the Novavax shot uses a more traditional type of technology based on proteins and has been shown to be as much as 90.4 per cent effective in trials, including against previous variants of concern. 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The Covid-19 vaccine, also known as Nuvaxovid, would be the Maryland-based company’s first marketed product after more than three decades in business.</p>\n<p>A meeting of an EMA panel has been scheduled for Monday, the agency said, adding that it would communicate more details on that day provided there was a conclusion.</p>\n<p>Separately, the WHO’s expert panel on vaccines met on Thursday to draft recommendations for use of the vaccine, with the WHO saying it would release its position “in the coming days”.</p>\n<p>WHO approval could come once the health body issued its own emergency use listing, or if the EMA gave it a conditional marketing authorisation, people familiar with the matter said.</p>\n<p>The step would allow deliveries to begin via global vaccine access scheme Covax. Together with the Serum Institute of India, Novavax has a commitment to supply Covax with 1.1bn doses.</p>\n<p>Two people familiar with both approval processes said there were still some “open questions” on manufacturing, but that the EMA should be able to issue a conditional approval. The open questions include so-called potency assays and drug substance characterisation — in essence, the ability of Novavax to ensure the product is the same everywhere and the same as that used in clinical studies.</p>\n<p>The people said Novavax had acknowledged these points in meetings and was working to address them.</p>\n<p>“It’s nothing serious. It’s not different from situations we have seen with previous vaccines,” one of the people said, while also cautioning that an approval was not certain.</p>\n<p>Novavax said both approval processes would consider extensive data on manufacturing as well as clinical and pre-clinical data. The company was “confident that the vaccine meets the stringent regulatory quality, safety and efficacy specifications” needed for authorisation by the WHO and the EMA and it looked forward to their decisions.</p>\n<p>The EMA declined to comment. The WHO said it would release its position “in the coming days”.</p>\n<p>One of the people added that the EMA was “racing against time” as the vaccine, which would initially only be approved for a primary series or the first two shots for someone who has not been vaccinated, could play “an important role” this winter.</p>\n<p>The Novavax shot has already been approved in the Philippines and Indonesia and the drugmaker has filed for approval in the UK. The company also expects to submit a complete application to the US Food and Drug Administration by year’s end.</p>\n<p>In contrast to the novel mRNA vaccines made by Moderna and Pfizer, the Novavax shot uses a more traditional type of technology based on proteins and has been shown to be as much as 90.4 per cent effective in trials, including against previous variants of concern. The company is now testing its efficacy against the new Omicron variant.</p>","source":"lsy1580170736413","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>WHO and EMA could approve Novavax Covid vaccine next week</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\">\nWHO and EMA could approve Novavax Covid vaccine next week\n</h2>\n\n<h4 class=\"meta\">\n\n\n2021-12-17 07:21 GMT+8&nbsp;&nbsp;&nbsp;<a href=https://www.ft.com/content/a938950e-7f97-46d6-a22c-6933c5634842><strong>Financial Times </strong></a>\n\n\n</h4>\n\n</header>\n<article>\n<div>\n<p>US drugmaker ‘confident’ as health bodies signal decisions are on the horizon\nMedical laboratory scientist Aniela Sobel tests serology samples from the Novavax phase 3 clinical trial in Seattle, ...</p>\n\n<a href=\"https://www.ft.com/content/a938950e-7f97-46d6-a22c-6933c5634842\">Web Link</a>\n\n</div>\n\n\n</article>\n</div>\n</body>\n</html>\n","type":0,"thumbnail":"","relate_stocks":{"NVAX":"诺瓦瓦克斯医药"},"source_url":"https://www.ft.com/content/a938950e-7f97-46d6-a22c-6933c5634842","is_english":true,"share_image_url":"https://static.laohu8.com/e9f99090a1c2ed51c021029395664489","article_id":"1116963836","content_text":"US drugmaker ‘confident’ as health bodies signal decisions are on the horizon\nMedical laboratory scientist Aniela Sobel tests serology samples from the Novavax phase 3 clinical trial in Seattle, Washington © Karen Ducey/Getty\nThe approvals would provide the US drugmaker with a significant boost after months of delays and share price volatility amid manufacturing issues. The Covid-19 vaccine, also known as Nuvaxovid, would be the Maryland-based company’s first marketed product after more than three decades in business.\nA meeting of an EMA panel has been scheduled for Monday, the agency said, adding that it would communicate more details on that day provided there was a conclusion.\nSeparately, the WHO’s expert panel on vaccines met on Thursday to draft recommendations for use of the vaccine, with the WHO saying it would release its position “in the coming days”.\nWHO approval could come once the health body issued its own emergency use listing, or if the EMA gave it a conditional marketing authorisation, people familiar with the matter said.\nThe step would allow deliveries to begin via global vaccine access scheme Covax. Together with the Serum Institute of India, Novavax has a commitment to supply Covax with 1.1bn doses.\nTwo people familiar with both approval processes said there were still some “open questions” on manufacturing, but that the EMA should be able to issue a conditional approval. The open questions include so-called potency assays and drug substance characterisation — in essence, the ability of Novavax to ensure the product is the same everywhere and the same as that used in clinical studies.\nThe people said Novavax had acknowledged these points in meetings and was working to address them.\n“It’s nothing serious. It’s not different from situations we have seen with previous vaccines,” one of the people said, while also cautioning that an approval was not certain.\nNovavax said both approval processes would consider extensive data on manufacturing as well as clinical and pre-clinical data. The company was “confident that the vaccine meets the stringent regulatory quality, safety and efficacy specifications” needed for authorisation by the WHO and the EMA and it looked forward to their decisions.\nThe EMA declined to comment. The WHO said it would release its position “in the coming days”.\nOne of the people added that the EMA was “racing against time” as the vaccine, which would initially only be approved for a primary series or the first two shots for someone who has not been vaccinated, could play “an important role” this winter.\nThe Novavax shot has already been approved in the Philippines and Indonesia and the drugmaker has filed for approval in the UK. The company also expects to submit a complete application to the US Food and Drug Administration by year’s end.\nIn contrast to the novel mRNA vaccines made by Moderna and Pfizer, the Novavax shot uses a more traditional type of technology based on proteins and has been shown to be as much as 90.4 per cent effective in trials, including against previous variants of concern. The company is now testing its efficacy against the new Omicron variant.","news_type":1},"isVote":1,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"tweetType":1,"langContent":"EN"}],"hasMoreComments":true,"newsSizeData":{"likeSize":72,"commentSize":0,"repostSize":0,"favoriteSize":0,"likeStatus":false,"favoriteStatus":false}}