Like ty_老虎社区_美港股上老虎

inv3st
2021-12-21

Like ty

Aquestive sheds a third after receiving FDA response for Libervant application

Aquestive Therapeutics drops nearly 30% premarket after receiving FDA notification regarding the rev

Aquestive sheds a third after receiving FDA response for Libervant application

免责声明：上述内容仅代表发帖人个人观点，不构成本平台的任何投资建议。

推荐
最新

暂无评论

热议股票

关于我们·老虎社区守则·老虎社区账号管理规范·老虎社区服务协议·老虎社区隐私政策

公司名称：北京至简风宜信息技术有限公司

违法和不良信息投诉：010-5681-3562（工作时间9:30-18:30）

邮箱：service@laohu8.com

营业执照：91110105MA01A4U55R

ICP备：京ICP备18016422号

网安备：京公网安备11010502036490

关注我们

{"i18n":{"language":"zh_CN"},"data":{"magic":2,"id":693752903,"tweetId":"693752903","gmtCreate":1640086833295,"gmtModify":1640086852941,"author":{"id":3577773488711202,"idStr":"3577773488711202","authorId":3577773488711202,"authorIdStr":"3577773488711202","name":"inv3st","avatar":"https://static.tigerbbs.com/efb6f0592ef761afbf6bab2267a2e76e","vip":1,"userType":1,"introduction":"","boolIsFan":false,"boolIsHead":false,"crmLevel":2,"crmLevelSwitch":0,"individualDisplayBadges":[],"fanSize":28,"starInvestorFlag":false},"themes":[],"images":[],"coverImages":[],"extraTitle":"","html":"<html><head></head><body><p>Like ty</p></body></html>","htmlText":"<html><head></head><body><p>Like ty</p></body></html>","text":"Like ty","highlighted":1,"essential":1,"paper":1,"likeSize":7,"commentSize":2,"repostSize":0,"favoriteSize":0,"link":"https://laohu8.com/post/693752903","repostId":1180762572,"repostType":4,"repost":{"id":"1180762572","pubTimestamp":1640086307,"share":"https://www.laohu8.com/m/news/1180762572?lang=&edition=full","pubTime":"2021-12-21 19:31","market":"us","language":"en","title":"Aquestive sheds a third after receiving FDA response for Libervant application","url":"https://stock-news.laohu8.com/highlight/detail?id=1180762572","media":"seekingalpha","summary":"Aquestive Therapeutics drops nearly 30% premarket after receiving FDA notification regarding the rev","content":"<p>Aquestive Therapeutics&nbsp;drops&nbsp;nearly 30% premarket&nbsp;after&nbsp;receiving&nbsp;FDA notification regarding the review of the New Drug Application (NDA) for Libervant (diazepam) Buccal Film for the treatment of breakthrough seizures and seizure clusters.</p>\n<p>The notice stated, \"the Agency is still considering the regulatory issues related to the approvability of Libervant, and will not be ready to take an action by December 23, 2021. No additional information is needed from you at this time. We are currently unable to provide an estimate of the timing of an expected action; however, we will provide any updates we can as they are available.”</p>\n<p>The company is currently reaching out to the FDA to seek further clarity.</p>\n<p>In July 2021, the FDA accepted the NDA for Libervant and assigned a&nbsp;PDUFA target goal date of December 23, 2021.</p>\n<p>The Company continues to advance AQST-109 as it began the EPIPHAST study, with results expected in H1 2022.</p>","source":"seekingalpha","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>Aquestive sheds a third after receiving FDA response for Libervant application</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\">\nAquestive sheds a third after receiving FDA response for Libervant application\n</h2>\n\n<h4 class=\"meta\">\n\n\n2021-12-21 19:31 GMT+8&nbsp;&nbsp;&nbsp;<a href=https://seekingalpha.com/news/3782227-aquestive-sheds-a-third-after-receiving-fda-response-for-libervant-application><strong>seekingalpha</strong></a>\n\n\n</h4>\n\n</header>\n<article>\n<div>\n<p>Aquestive Therapeutics drops nearly 30% premarket after receiving FDA notification regarding the review of the New Drug Application (NDA) for Libervant (diazepam) Buccal Film for the treatment of ...</p>\n\n<a href=\"https://seekingalpha.com/news/3782227-aquestive-sheds-a-third-after-receiving-fda-response-for-libervant-application\">Web Link</a>\n\n</div>\n\n\n</article>\n</div>\n</body>\n</html>\n","type":0,"thumbnail":"","relate_stocks":{"AQST":"Aquestive Therapeutics Inc."},"source_url":"https://seekingalpha.com/news/3782227-aquestive-sheds-a-third-after-receiving-fda-response-for-libervant-application","is_english":true,"share_image_url":"https://static.laohu8.com/5a36db9d73b4222bc376d24ccc48c8a4","article_id":"1180762572","content_text":"Aquestive Therapeutics drops nearly 30% premarket after receiving FDA notification regarding the review of the New Drug Application (NDA) for Libervant (diazepam) Buccal Film for the treatment of breakthrough seizures and seizure clusters.\nThe notice stated, \"the Agency is still considering the regulatory issues related to the approvability of Libervant, and will not be ready to take an action by December 23, 2021. No additional information is needed from you at this time. We are currently unable to provide an estimate of the timing of an expected action; however, we will provide any updates we can as they are available.”\nThe company is currently reaching out to the FDA to seek further clarity.\nIn July 2021, the FDA accepted the NDA for Libervant and assigned a PDUFA target goal date of December 23, 2021.\nThe Company continues to advance AQST-109 as it began the EPIPHAST study, with results expected in H1 2022.","news_type":1},"isVote":1,"tweetType":1,"viewCount":962,"commentLimit":10,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"symbols":[],"verified":2,"subType":0,"readableState":1,"langContent":"CN","currentLanguage":"CN","warmUpFlag":false,"orderFlag":false,"shareable":true,"causeOfNotShareable":"","featuresForAnalytics":[],"commentAndTweetFlag":false,"andRepostAutoSelectedFlag":false,"upFlag":false,"length":6,"xxTargetLangEnum":"ZH_CN"},"commentList":[],"hasMoreComment":false,"orderType":2}

Aquestive sheds a third after receiving FDA response for Libervant application

评论（2）

热议股票