Aquestive sheds a third after receiving FDA response for Libervant application_老虎社区_美港股上老虎

Aquestive sheds a third after receiving FDA response for Libervant application

seekingalpha2021-12-21

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 ...

网页链接

免责声明：本文观点仅代表作者个人观点，不构成本平台的投资建议，本平台不对文章信息准确性、完整性和及时性做出任何保证，亦不对因使用或信赖文章信息引发的任何损失承担责任。

BKT
·2021-12-21
Good. Pls like thanks.
回复
1
举报
Dsd
·2021-12-21
...
回复
3
举报
boonwt
·2021-12-21
Hmm
回复
5
举报
收起
- RaymondLim:
  ok
  2021-12-21
  回复
  举报
NPC69
·2021-12-21
K
回复
6
举报
收起
- RaymondLim:
  ok
  2021-12-21
  回复
  举报
- jingabel:
  ok
  2021-12-21
  回复
  举报
LY1970
·2021-12-21
Hello
回复
4
举报
收起
- Dsd:
  ...
  2021-12-21
  回复
  举报
- LY1970:
  Bj
  2021-12-21
  回复
  举报
auahau
·2021-12-21
wow
回复
5
举报
收起
- thatsy:
  Paper hands
  2021-12-21
  回复
  举报
FunnyFun
·2021-12-21
LIKE
回复
7
举报
收起
- edwinong:
  ok
  2021-12-21
  回复
  举报
ahBern
·2021-12-21
Like
回复
6
举报
Zero_onezero
·2021-12-21
Woo
回复
8
举报
收起
- ahBern:
  Ok
  2021-12-21
  回复
  举报
inv3st
·2021-12-21
Like ty
回复
7
举报
收起
- Zero_onezero:
  ye
  2021-12-21
  回复
  举报
- cgoh:
  👍🏼
  2021-12-21
  回复
  举报
CloudStrife
·2021-12-21
Help like pls [Shy]
回复
9
举报
收起
- DylanT:
  done
  2021-12-21
  回复
  举报
- Muan:
  like
  2021-12-21
  回复
  举报
- JemLIm:
  ok
  2021-12-21
  回复
  举报
JoeK
·2021-12-21
Ok
回复
10
举报
收起
- JoeK:
  ok
  2021-12-21
  回复
  举报

热议股票

7x24

全部

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":{"share":"https://www.laohu8.com/m/news/1180762572?lang=zh_CN&edition=full","thumbnail":"","is_english":true,"pubTime":"2021-12-21 19:31","share_image_url":"https://static.laohu8.com/5a36db9d73b4222bc376d24ccc48c8a4","id":"1180762572","market":"us","top_or_hot":-1,"title":"Aquestive sheds a third after receiving FDA response for Libervant application","media":"seekingalpha","content":"<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\">网页链接</a>\n\n</div>\n","source":"seekingalpha","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\">网页链接</a>\n\n</div>\n\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"AQST","symbol_name":"Aquestive Therapeutics Inc.","start_time":0,"source_url":"https://seekingalpha.com/news/3782227-aquestive-sheds-a-third-after-receiving-fda-response-for-libervant-application","article_id":"1180762572","we_media_id":null,"thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=1180762572","pubTimestamp":1640086307,"sourceInfo":{"source_id":"seekingalpha","name":"Seeking Alpha"},"weMediaInfo":null,"summary":"Aquestive Therapeutics drops nearly 30% premarket after receiving FDA notification regarding the rev","collect":0,"end_time":0,"defaultTopTitle":"seekingalpha.com","property":[],"viewcount":null,"language":"en","relate_stocks":{"AQST":"Aquestive Therapeutics Inc."},"translate_title":"在收到FDA对Libervant申请的回应后，Aquestive脱落了三分之一","themeId":null,"isJumpTheme":false,"ttsUrl":null,"symbols_score_info":{"AQST":0.9},"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.","kind":null,"is_publish_news":true,"is_publish_highlight":false,"is_publish_live":null,"is_publish_wemedia":null,"editions":null,"column":"","sentiment":"","news_tag":"","news_rank":0,"symbols":[],"gpt_button":1},"commentList":[{"id":691046894,"gmtCreate":1640102331922,"gmtModify":1640102332112,"author":{"id":"3570853427202414","authorId":"3570853427202414","name":"BKT","avatar":"https://static.laohu8.com/default-avatar.jpg","vip":1,"crmLevel":2,"crmLevelSwitch":0},"htmlText":"Good. Pls like thanks.","listText":"Good. Pls like thanks.","text":"Good. Pls like thanks.","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":1,"commentSize":0,"repostSize":0,"link":"https://laohu8.com/post/691046894","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,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"tweetType":1,"langContent":"CN"},{"id":693747941,"gmtCreate":1640089925284,"gmtModify":1640089925439,"author":{"id":"3581036261146444","authorId":"3581036261146444","name":"Dsd","avatar":"https://static.tigerbbs.com/2a1957746498df0232ae53ac81018443","vip":1,"crmLevel":1,"crmLevelSwitch":0},"htmlText":"...","listText":"...","text":"...","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":3,"commentSize":0,"repostSize":0,"link":"https://laohu8.com/post/693747941","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,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"tweetType":1,"langContent":"CN"},{"id":693746556,"gmtCreate":1640089100605,"gmtModify":1640089100704,"author":{"id":"3582940622326289","authorId":"3582940622326289","name":"boonwt","avatar":"https://static.tigerbbs.com/e4d5c6d9b0cc6a1498dd442e0259cd8a","vip":1,"crmLevel":2,"crmLevelSwitch":0},"htmlText":"Hmm","listText":"Hmm","text":"Hmm","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":5,"commentSize":1,"repostSize":0,"link":"https://laohu8.com/post/693746556","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,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"tweetType":1,"comments":[{"id":7066516,"gmtCreate":1640090768655,"gmtModify":1640090768712,"authorId":3581634125853828,"author":{"id":3581634125853828,"authorId":3581634125853828,"name":"RaymondLim","avatar":"https://static.tigerbbs.com/d3081d4d67e2198188bc8039305c484f","vip":1,"crmLevel":3,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693746556,"type":1,"supId":0,"prevId":0,"content":"ok","text":"ok","html":"ok"}],"langContent":"CN"},{"id":693743161,"gmtCreate":1640088406990,"gmtModify":1640088407470,"author":{"id":"3584779133668268","authorId":"3584779133668268","name":"NPC69","avatar":"https://static.tigerbbs.com/47e7ac55312ae8dd1c9e7cb92adad089","vip":1,"crmLevel":5,"crmLevelSwitch":0},"htmlText":"K","listText":"K","text":"K","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":6,"commentSize":2,"repostSize":0,"link":"https://laohu8.com/post/693743161","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,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"tweetType":1,"comments":[{"id":7066515,"gmtCreate":1640090760919,"gmtModify":1640090761018,"authorId":3581634125853828,"author":{"id":3581634125853828,"authorId":3581634125853828,"name":"RaymondLim","avatar":"https://static.tigerbbs.com/d3081d4d67e2198188bc8039305c484f","vip":1,"crmLevel":3,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693743161,"type":1,"supId":0,"prevId":0,"content":"<u>ok</u>","text":"<u>ok</u>","html":"<u>ok</u>"},{"id":7066409,"gmtCreate":1640089535076,"gmtModify":1640089535110,"authorId":3579683280519440,"author":{"id":3579683280519440,"authorId":3579683280519440,"name":"jingabel","avatar":"https://static.tigerbbs.com/5109716c64f0b691a5098e4d5397ffc2","vip":1,"crmLevel":2,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693743161,"type":1,"supId":0,"prevId":0,"content":"ok","text":"ok","html":"ok"}],"langContent":"CN"},{"id":693749480,"gmtCreate":1640088381052,"gmtModify":1640088381329,"author":{"id":"3581643786644012","authorId":"3581643786644012","name":"LY1970","avatar":"https://static.tigerbbs.com/99deb9932439b87c6072806b53ff4f0b","vip":1,"crmLevel":4,"crmLevelSwitch":0},"htmlText":"Hello","listText":"Hello","text":"Hello","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":4,"commentSize":2,"repostSize":0,"link":"https://laohu8.com/post/693749480","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,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"tweetType":1,"comments":[{"id":7066436,"gmtCreate":1640089939878,"gmtModify":1640089939977,"authorId":3581036261146444,"author":{"id":3581036261146444,"authorId":3581036261146444,"name":"Dsd","avatar":"https://static.tigerbbs.com/2a1957746498df0232ae53ac81018443","vip":1,"crmLevel":1,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693749480,"type":1,"supId":0,"prevId":0,"content":"...","text":"...","html":"..."},{"id":7066309,"gmtCreate":1640088386792,"gmtModify":1640088386881,"authorId":3581643786644012,"author":{"id":3581643786644012,"authorId":3581643786644012,"name":"LY1970","avatar":"https://static.tigerbbs.com/99deb9932439b87c6072806b53ff4f0b","vip":1,"crmLevel":4,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693749480,"type":1,"supId":0,"prevId":0,"content":"Bj","text":"Bj","html":"Bj"}],"langContent":"CN"},{"id":693749815,"gmtCreate":1640088326944,"gmtModify":1640088327196,"author":{"id":"3575098313311401","authorId":"3575098313311401","name":"auahau","avatar":"https://static.tigerbbs.com/51a7e0e9a14e5faa1ff39d0755eb5e92","vip":1,"crmLevel":2,"crmLevelSwitch":0},"htmlText":"wow","listText":"wow","text":"wow","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":5,"commentSize":1,"repostSize":0,"link":"https://laohu8.com/post/693749815","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,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"tweetType":1,"comments":[{"id":7066307,"gmtCreate":1640088377846,"gmtModify":1640088377882,"authorId":3553846715363515,"author":{"id":3553846715363515,"authorId":3553846715363515,"name":"thatsy","avatar":"https://static.tigerbbs.com/f26fbbdbb8bc4a4041112e5874d1041e","vip":1,"crmLevel":3,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693749815,"type":1,"supId":0,"prevId":0,"content":"Paper hands","text":"Paper hands","html":"Paper hands"}],"langContent":"CN"},{"id":693755462,"gmtCreate":1640087246361,"gmtModify":1640087246703,"author":{"id":"3581664026895626","authorId":"3581664026895626","name":"FunnyFun","avatar":"https://static.tigerbbs.com/e07aca58746125ec6ef6115042d363e9","vip":1,"crmLevel":2,"crmLevelSwitch":0},"htmlText":"LIKE","listText":"LIKE","text":"LIKE","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":7,"commentSize":1,"repostSize":0,"link":"https://laohu8.com/post/693755462","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,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"tweetType":1,"comments":[{"id":7066195,"gmtCreate":1640087355639,"gmtModify":1640087355674,"authorId":3581723087274150,"author":{"id":3581723087274150,"authorId":3581723087274150,"name":"edwinong","avatar":"https://static.tigerbbs.com/d42f3dae28f8c1740e66011b66f51ccd","vip":1,"crmLevel":2,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693755462,"type":1,"supId":0,"prevId":0,"content":"<u>ok</u>","text":"<u>ok</u>","html":"<u>ok</u>"}],"langContent":"CN"},{"id":693755346,"gmtCreate":1640087042481,"gmtModify":1640087042760,"author":{"id":"4087650318161980","authorId":"4087650318161980","name":"ahBern","avatar":"https://static.tigerbbs.com/88263929bb1a9cc8c5ea90409c5bd436","vip":1,"crmLevel":3,"crmLevelSwitch":0},"htmlText":"Like","listText":"Like","text":"Like","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":6,"commentSize":0,"repostSize":0,"link":"https://laohu8.com/post/693755346","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,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"tweetType":1,"langContent":"CN"},{"id":693752403,"gmtCreate":1640086989184,"gmtModify":1640086989507,"author":{"id":"3581743394055717","authorId":"3581743394055717","name":"Zero_onezero","avatar":"https://static.tigerbbs.com/f93660d80ec28ae67a094cb5c0c44350","vip":1,"crmLevel":2,"crmLevelSwitch":0},"htmlText":"Woo","listText":"Woo","text":"Woo","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":8,"commentSize":1,"repostSize":0,"link":"https://laohu8.com/post/693752403","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,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"tweetType":1,"comments":[{"id":7066165,"gmtCreate":1640087047518,"gmtModify":1640087047611,"authorId":4087650318161980,"author":{"id":4087650318161980,"authorId":4087650318161980,"name":"ahBern","avatar":"https://static.tigerbbs.com/88263929bb1a9cc8c5ea90409c5bd436","vip":1,"crmLevel":3,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693752403,"type":1,"supId":0,"prevId":0,"content":"<u>Ok</u>","text":"<u>Ok</u>","html":"<u>Ok</u>"}],"langContent":"CN"},{"id":693752903,"gmtCreate":1640086833295,"gmtModify":1640086852941,"author":{"id":"3577773488711202","authorId":"3577773488711202","name":"inv3st","avatar":"https://static.tigerbbs.com/efb6f0592ef761afbf6bab2267a2e76e","vip":1,"crmLevel":3,"crmLevelSwitch":0},"htmlText":"Like ty","listText":"Like ty","text":"Like ty","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":7,"commentSize":2,"repostSize":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,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"tweetType":1,"comments":[{"id":7066159,"gmtCreate":1640086984546,"gmtModify":1640086984650,"authorId":3581743394055717,"author":{"id":3581743394055717,"authorId":3581743394055717,"name":"Zero_onezero","avatar":"https://static.tigerbbs.com/f93660d80ec28ae67a094cb5c0c44350","vip":1,"crmLevel":2,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693752903,"type":1,"supId":0,"prevId":0,"content":"<u>ye</u>","text":"<u>ye</u>","html":"<u>ye</u>"},{"id":7066155,"gmtCreate":1640086952981,"gmtModify":1640086953015,"authorId":4087794564530700,"author":{"id":4087794564530700,"authorId":4087794564530700,"name":"cgoh","avatar":"https://static.laohu8.com/default-avatar.jpg","vip":1,"crmLevel":3,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693752903,"type":1,"supId":0,"prevId":0,"content":"👍🏼","text":"👍🏼","html":"👍🏼"}],"langContent":"CN"},{"id":693756521,"gmtCreate":1640086674721,"gmtModify":1640086675179,"author":{"id":"4088395966157920","authorId":"4088395966157920","name":"CloudStrife","avatar":"https://static.tigerbbs.com/c8b6c92f874979adf46532fabf329bd9","vip":1,"crmLevel":7,"crmLevelSwitch":0},"htmlText":"Help like pls [Shy]&nbsp;","listText":"Help like pls [Shy]&nbsp;","text":"Help like pls [Shy]","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":9,"commentSize":3,"repostSize":0,"link":"https://laohu8.com/post/693756521","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,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"tweetType":1,"comments":[{"id":7066153,"gmtCreate":1640086940863,"gmtModify":1640086940970,"authorId":3582541483650512,"author":{"id":3582541483650512,"authorId":3582541483650512,"name":"DylanT","avatar":"https://static.laohu8.com/default-avatar.jpg","vip":1,"crmLevel":2,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693756521,"type":1,"supId":0,"prevId":0,"content":"<u>done</u>","text":"<u>done</u>","html":"<u>done</u>"},{"id":7066140,"gmtCreate":1640086793495,"gmtModify":1640086793590,"authorId":3567122626731680,"author":{"id":3567122626731680,"authorId":3567122626731680,"name":"Muan","avatar":"https://static.tigerbbs.com/e57898e50017c4ba74bca13a29623eab","vip":1,"crmLevel":2,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693756521,"type":1,"supId":0,"prevId":0,"content":"<u>like</u>","text":"<u>like</u>","html":"<u>like</u>"},{"id":7066134,"gmtCreate":1640086739843,"gmtModify":1640086739937,"authorId":3574813808924805,"author":{"id":3574813808924805,"authorId":3574813808924805,"name":"JemLIm","avatar":"https://static.tigerbbs.com/ee9608155c1d123b0bf9fc773916aac7","vip":1,"crmLevel":2,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693756521,"type":1,"supId":0,"prevId":0,"content":"<u>ok</u>","text":"<u>ok</u>","html":"<u>ok</u>"}],"langContent":"CN"},{"id":693756129,"gmtCreate":1640086628251,"gmtModify":1640086628616,"author":{"id":"3575261937306050","authorId":"3575261937306050","name":"JoeK","avatar":"https://static.tigerbbs.com/162445e8b6a553bd412b8a06e3f44c9e","vip":1,"crmLevel":6,"crmLevelSwitch":0},"htmlText":"Ok","listText":"Ok","text":"Ok","images":[],"top":1,"highlighted":1,"essential":1,"paper":1,"likeSize":10,"commentSize":1,"repostSize":0,"link":"https://laohu8.com/post/693756129","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,"likeStatus":false,"favoriteStatus":false,"reportStatus":false,"tweetType":1,"comments":[{"id":7066121,"gmtCreate":1640086634114,"gmtModify":1640086634140,"authorId":3575261937306050,"author":{"id":3575261937306050,"authorId":3575261937306050,"name":"JoeK","avatar":"https://static.tigerbbs.com/162445e8b6a553bd412b8a06e3f44c9e","vip":1,"crmLevel":6,"crmLevelSwitch":0,"individualDisplayBadges":[]},"repliedAuthorId":0,"objectId":693756129,"type":1,"supId":0,"prevId":0,"content":"<u>ok</u>","text":"<u>ok</u>","html":"<u>ok</u>"}],"langContent":"CN"}],"hasMoreComments":true,"newsSizeData":{"likeSize":86,"commentSize":12,"repostSize":0,"favoriteSize":0,"likeStatus":false,"favoriteStatus":false}}