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合纵连横

合纵连横

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IP属地：北京

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0勋章

2021-04-15

$怪兽充电(EM)$怪兽啊不容易啊

2021-05-20

$涂鸦智能(TUYA)$24怎么不平？设置了啊

2021-08-04

！这是我关注的

2021-04-16

$知乎(ZH)$知乎啊很久了

01-25

$小鹏汽车(XPEV)$ 可以涨

2022-07-15

这篇文章不错，转发给大家看

Needham：下调Ironsource Ltd评级至“持有”

2022-06-08

这篇文章不错，转发给大家看

诺瓦瓦克斯(NVAX.US)新冠疫苗获得FDA咨询委员会的批准建议

2021-03-19

哔滴哔滴打新

去老虎APP查看更多动态

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08:25","market":"sh","language":"zh","title":"诺瓦瓦克斯(NVAX.US)新冠疫苗获得FDA咨询委员会的批准建议","url":"https://stock-news.laohu8.com/highlight/detail?id=2241993836","media":"智通财经","summary":"智通财经APP获悉，经过美国食品药品监督管理局咨询委员会的审查，诺瓦瓦克斯的新冠疫苗获得了在美国的紧急使用授权申请。FDA的独立疫苗专家委员会以21票赞成、0票反对、1票弃权的结果，建议批准在美国使用这种疫苗。此前，FDA召开了一整天的公开会议，对诺瓦瓦克斯新冠疫苗的安全性和有效性数据进行了权衡。FDA通常会遵循委员会的建议，尽管它没有义务这样做。该机构可能最早于本周批准诺瓦瓦克斯疫苗在美国销售。","content":"<html><body><p>智通财经APP获悉，经过美国食品药品监督管理局(FDA)咨询委员会的审查，诺瓦瓦克斯(NVAX.US)的新冠疫苗获得了在美国的紧急使用授权申请(EUA)。</p><p>FDA的独立疫苗专家委员会以21票赞成、0票反对、1票弃权的结果，建议批准在美国使用这种疫苗。</p><p>此前，FDA召开了一整天的公开会议，对诺瓦瓦克斯新冠疫苗的安全性和有效性数据进行了权衡。FDA通常会遵循委员会的建议，尽管它没有义务这样做。该机构可能最早于本周批准诺瓦瓦克斯疫苗在美国销售。</p><p>诺瓦瓦克斯的疫苗将是美国批准使用的第四种新冠疫苗，也是在2021年2月强生疫苗获得批准后的第一种新疫苗。</p><p>诺瓦瓦克斯是美国政府2020年研发新冠疫苗竞赛的早期参与者之一，从“曲速行动”获得了18亿美元的资金。然而，该公司花了一年多的时间才开始生产，其临床试验数据出现得比<a href=\"https://laohu8.com/S/PFE\">辉瑞</a>和Moderna晚得多。</p></body></html>","source":"stock_zhitongcaijing","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>诺瓦瓦克斯(NVAX.US)新冠疫苗获得FDA咨询委员会的批准建议</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; 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href=http://www.zhitongcaijing.com/content/detail/735196.html><strong>智通财经</strong></a>\n\n\n</h4>\n\n</header>\n<article>\n<div>\n<p>智通财经APP获悉，经过美国食品药品监督管理局(FDA)咨询委员会的审查，诺瓦瓦克斯(NVAX.US)的新冠疫苗获得了在美国的紧急使用授权申请(EUA)。FDA的独立疫苗专家委员会以21票赞成、0票反对、1票弃权的结果，建议批准在美国使用这种疫苗。此前，FDA召开了一整天的公开会议，对诺瓦瓦克斯新冠疫苗的安全性和有效性数据进行了权衡。FDA通常会遵循委员会的建议，尽管它没有义务这样做。该机构可能...</p>\n\n<a href=\"http://www.zhitongcaijing.com/content/detail/735196.html\">Web Link</a>\n\n</div>\n\n\n</article>\n</div>\n</body>\n</html>\n","type":0,"thumbnail":"","relate_stocks":{"BK4139":"生物科技","NVAX":"诺瓦瓦克斯医药"},"source_url":"http://www.zhitongcaijing.com/content/detail/735196.html","is_english":false,"share_image_url":"https://static.laohu8.com/e9f99090a1c2ed51c021029395664489","article_id":"2241993836","content_text":"智通财经APP获悉，经过美国食品药品监督管理局(FDA)咨询委员会的审查，诺瓦瓦克斯(NVAX.US)的新冠疫苗获得了在美国的紧急使用授权申请(EUA)。FDA的独立疫苗专家委员会以21票赞成、0票反对、1票弃权的结果，建议批准在美国使用这种疫苗。此前，FDA召开了一整天的公开会议，对诺瓦瓦克斯新冠疫苗的安全性和有效性数据进行了权衡。FDA通常会遵循委员会的建议，尽管它没有义务这样做。该机构可能最早于本周批准诺瓦瓦克斯疫苗在美国销售。诺瓦瓦克斯的疫苗将是美国批准使用的第四种新冠疫苗，也是在2021年2月强生疫苗获得批准后的第一种新疫苗。诺瓦瓦克斯是美国政府2020年研发新冠疫苗竞赛的早期参与者之一，从“曲速行动”获得了18亿美元的资金。然而，该公司花了一年多的时间才开始生产，其临床试验数据出现得比辉瑞和Moderna晚得多。","news_type":1},"isVote":1,"tweetType":1,"viewCount":675,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"CN","totalScore":0},{"id":890168098,"gmtCreate":1628087282214,"gmtModify":1628087282214,"author":{"id":"3578628887495303","authorId":"3578628887495303","name":"合纵连横","avatar":"https://static.tigerbbs.com/f59efc3c7e2502db83c8c303d40e8f57","crmLevel":2,"crmLevelSwitch":0,"followedFlag":false},"themes":[],"htmlText":"！这是我关注的","listText":"！这是我关注的","text":"！这是我关注的","images":[{"img":"https://static.tigerbbs.com/b1a04d4d35d28f2d5b42804e86a20fcf","width":"1080","height":"1920"}],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":1,"commentSize":0,"repostSize":0,"link":"https://laohu8.com/post/890168098","isVote":1,"tweetType":1,"viewCount":697,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":1,"langContent":"CN","totalScore":0},{"id":130155039,"gmtCreate":1621520333821,"gmtModify":1621520333821,"author":{"id":"3578628887495303","authorId":"3578628887495303","name":"合纵连横","avatar":"https://static.tigerbbs.com/f59efc3c7e2502db83c8c303d40e8f57","crmLevel":2,"crmLevelSwitch":0,"followedFlag":false},"themes":[],"htmlText":"<a 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08:25","market":"sh","language":"zh","title":"诺瓦瓦克斯(NVAX.US)新冠疫苗获得FDA咨询委员会的批准建议","url":"https://stock-news.laohu8.com/highlight/detail?id=2241993836","media":"智通财经","summary":"智通财经APP获悉，经过美国食品药品监督管理局咨询委员会的审查，诺瓦瓦克斯的新冠疫苗获得了在美国的紧急使用授权申请。FDA的独立疫苗专家委员会以21票赞成、0票反对、1票弃权的结果，建议批准在美国使用这种疫苗。此前，FDA召开了一整天的公开会议，对诺瓦瓦克斯新冠疫苗的安全性和有效性数据进行了权衡。FDA通常会遵循委员会的建议，尽管它没有义务这样做。该机构可能最早于本周批准诺瓦瓦克斯疫苗在美国销售。","content":"<html><body><p>智通财经APP获悉，经过美国食品药品监督管理局(FDA)咨询委员会的审查，诺瓦瓦克斯(NVAX.US)的新冠疫苗获得了在美国的紧急使用授权申请(EUA)。</p><p>FDA的独立疫苗专家委员会以21票赞成、0票反对、1票弃权的结果，建议批准在美国使用这种疫苗。</p><p>此前，FDA召开了一整天的公开会议，对诺瓦瓦克斯新冠疫苗的安全性和有效性数据进行了权衡。FDA通常会遵循委员会的建议，尽管它没有义务这样做。该机构可能最早于本周批准诺瓦瓦克斯疫苗在美国销售。</p><p>诺瓦瓦克斯的疫苗将是美国批准使用的第四种新冠疫苗，也是在2021年2月强生疫苗获得批准后的第一种新疫苗。</p><p>诺瓦瓦克斯是美国政府2020年研发新冠疫苗竞赛的早期参与者之一，从“曲速行动”获得了18亿美元的资金。然而，该公司花了一年多的时间才开始生产，其临床试验数据出现得比<a href=\"https://laohu8.com/S/PFE\">辉瑞</a>和Moderna晚得多。</p></body></html>","source":"stock_zhitongcaijing","collect":0,"html":"<!DOCTYPE html>\n<html>\n<head>\n<meta http-equiv=\"Content-Type\" content=\"text/html; 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href=http://www.zhitongcaijing.com/content/detail/735196.html><strong>智通财经</strong></a>\n\n\n</h4>\n\n</header>\n<article>\n<div>\n<p>智通财经APP获悉，经过美国食品药品监督管理局(FDA)咨询委员会的审查，诺瓦瓦克斯(NVAX.US)的新冠疫苗获得了在美国的紧急使用授权申请(EUA)。FDA的独立疫苗专家委员会以21票赞成、0票反对、1票弃权的结果，建议批准在美国使用这种疫苗。此前，FDA召开了一整天的公开会议，对诺瓦瓦克斯新冠疫苗的安全性和有效性数据进行了权衡。FDA通常会遵循委员会的建议，尽管它没有义务这样做。该机构可能...</p>\n\n<a href=\"http://www.zhitongcaijing.com/content/detail/735196.html\">Web Link</a>\n\n</div>\n\n\n</article>\n</div>\n</body>\n</html>\n","type":0,"thumbnail":"","relate_stocks":{"BK4139":"生物科技","NVAX":"诺瓦瓦克斯医药"},"source_url":"http://www.zhitongcaijing.com/content/detail/735196.html","is_english":false,"share_image_url":"https://static.laohu8.com/e9f99090a1c2ed51c021029395664489","article_id":"2241993836","content_text":"智通财经APP获悉，经过美国食品药品监督管理局(FDA)咨询委员会的审查，诺瓦瓦克斯(NVAX.US)的新冠疫苗获得了在美国的紧急使用授权申请(EUA)。FDA的独立疫苗专家委员会以21票赞成、0票反对、1票弃权的结果，建议批准在美国使用这种疫苗。此前，FDA召开了一整天的公开会议，对诺瓦瓦克斯新冠疫苗的安全性和有效性数据进行了权衡。FDA通常会遵循委员会的建议，尽管它没有义务这样做。该机构可能最早于本周批准诺瓦瓦克斯疫苗在美国销售。诺瓦瓦克斯的疫苗将是美国批准使用的第四种新冠疫苗，也是在2021年2月强生疫苗获得批准后的第一种新疫苗。诺瓦瓦克斯是美国政府2020年研发新冠疫苗竞赛的早期参与者之一，从“曲速行动”获得了18亿美元的资金。然而，该公司花了一年多的时间才开始生产，其临床试验数据出现得比辉瑞和Moderna晚得多。","news_type":1},"isVote":1,"tweetType":1,"viewCount":675,"authorTweetTopStatus":1,"verified":2,"comments":[],"imageCount":0,"langContent":"CN","totalScore":0},{"id":350150702,"gmtCreate":1616168482406,"gmtModify":1616168482406,"author":{"id":"3578628887495303","authorId":"3578628887495303","name":"合纵连横","avatar":"https://static.tigerbbs.com/f59efc3c7e2502db83c8c303d40e8f57","crmLevel":2,"crmLevelSwitch":0,"followedFlag":false},"themes":[],"htmlText":"哔滴哔滴 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