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Aquestive Therapeutics Inc.

4.21

+0.33008.51%

Post-market: 4.20-0.0101-0.24%19:47 EDT

Volume:1.84M

Turnover:7.59M

Market Cap:513.63M

PE:-5.37

High:4.22

Open:3.91

Low:3.91

Close:3.88

52wk High:7.55

52wk Low:2.12

Shares:122.00M

Float Shares:115.00M

Volume Ratio:0.93

T/O Rate:1.60%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-0.7836

EPS(LYR):-0.7836

ROE:148.50%

ROA:-33.92%

PB:-15.26

PE(LYR):-5.37

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Overview Company News Filings

NASD Most Active Issues

Aquestive Therapeutics Inc : Leerink Partners Cuts Target Price to $7 From $11

THOMSON REUTERS

Aquestive Therapeutics (AQST) Is Down 39.4% After FDA Flags Deficiencies in Anaphylm Filing - What's Changed

Simply Wall St.

Benzinga Bulls And Bears: Chevron, Palantir, Aquestive — And Real Estate Stocks Plummet

Benzinga_recent_news

Aquestive Therapeutics Down Over 38%, on Track for Record Percent Decrease -- Data Talk

Crude Oil Rises Sharply; US Consumer Sentiment Edges Higher In January

Aquestive Stock Slides After FDA Flags Issues With Allergy Drug Application

Benzinga_recent_news

ARS Pharmaceuticals competitor gets FDA deficiency letter, says Raymond James

Aquestive Therapeutics Shares Plunge 37.2% After FDA Identifies Deficiencies in Marketing Application for Experimental Drug for Allergic Reactions

THOMSON REUTERS

BUZZ-U.S. STOCKS ON THE MOVE-Broadcom, home lenders, First Solar

Lake Street Reaffirms Their Buy Rating on Aquestive Therapeutics (AQST)

BUZZ-Aquestive Therapeutics falls as FDA flags issues with oral allergy drug

Aquestive Therapeutics Shares Down 48% Premarket After FDA Identifies Deficiencies in Co's Marketing Application for Its Experimental Drug for Allergic Reactions

THOMSON REUTERS

FDA Identifies Deficiencies in Aquestive Anaphylm Review, Approval Pending

Aquestive Therapeutics Expands Global Regulatory Efforts for Anaphylm

Aquestive Therapeutics Inc - Progresses Global Regulatory Expansion for Anaphylm

THOMSON REUTERS

Aquestive Therapeutics Announces Regulatory Development for Anaphylm™ (Dibutepinephrine) Sublingual Film and Provides Business Update

THOMSON REUTERS

Aquestive Therapeutics Inc - FDA Identifies Deficiencies in Anaphylm Nda

THOMSON REUTERS

Aquestive Therapeutics Inc - FDA Review of Anaphylm Nda Ongoing

THOMSON REUTERS

Needle‑Free Anaphylaxis Treatments Poised for Growth: Physician Survey Supports Buy Rating on Aquestive’s Anaphylm (AQST)

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42.27% at today's intraday low; largest intraday percent decrease since March 12, 2020, when it fell as much as 45.24%","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-2","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["AQST","BK4539","LENZ","BK4139","BK4007"],"gpt_icon":0},{"id":"2602087053","title":"Crude Oil Rises Sharply; US Consumer Sentiment Edges Higher In January","url":"https://stock-news.laohu8.com/highlight/detail?id=2602087053","media":"Benzinga","labels":["express"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2602087053?lang=en_us&edition=fundamental","pubTime":"2026-01-10 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Street Reaffirms Their Buy Rating on Aquestive Therapeutics (AQST)","url":"https://stock-news.laohu8.com/highlight/detail?id=2602937133","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2602937133?lang=en_us&edition=fundamental","pubTime":"2026-01-09 21:56","pubTimestamp":1767966985,"startTime":"0","endTime":"0","summary":"Lake Street analyst Thomas Flaten maintained a Buy rating on Aquestive Therapeutics today and set a price target of $8.00. According to TipRanks, F...","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/blurbs/lake-street-reaffirms-their-buy-rating-on-aquestive-therapeutics-aqst-blurbs-3?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":["rate"],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/blurbs/lake-street-reaffirms-their-buy-rating-on-aquestive-therapeutics-aqst-blurbs-3?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["AQST"],"gpt_icon":0},{"id":"2602731583","title":"BUZZ-Aquestive Therapeutics falls as FDA flags issues with oral allergy drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2602731583","media":"Reuters","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2602731583?lang=en_us&edition=fundamental","pubTime":"2026-01-09 20:27","pubTimestamp":1767961665,"startTime":"0","endTime":"0","summary":"BUZZ-Aquestive Therapeutics falls as FDA flags issues with oral allergy drug** Shares of drug developer Aquestive Therapeutics AQST.O fall 44% to $3.49 premarket** Co says it received a letter from the U.S. FDA highlighting issues with its new allergy treatment, Anaphylm** FDA raised concerns delaying talks on Anaphylm's labeling and marketing, per co** AQST's Anaphylm is a dissolvable film with epinephrine for severe allergic reactions - AQST** The FDA is expected to make a decision on Anaphylm by January 31, the scheduled action date** Co says if approved, it would be first oral alternative to epinephrine auto-injectors** As of last close, stock up ~81% over the past year   ","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260109:nL4N3YA0UP:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-2","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["AQST","BK4007"],"gpt_icon":0},{"id":"2602736623","title":"Aquestive Therapeutics Shares Down 48% Premarket After FDA Identifies Deficiencies in Co's Marketing Application for Its Experimental Drug for Allergic Reactions","url":"https://stock-news.laohu8.com/highlight/detail?id=2602736623","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2602736623?lang=en_us&edition=fundamental","pubTime":"2026-01-09 20:20","pubTimestamp":1767961218,"startTime":"0","endTime":"0","summary":null,"market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260109:nL4N3YA0UW:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"reuters_en_live","symbols":["BK4007","AQST"],"gpt_icon":0},{"id":"2602988378","title":"FDA Identifies Deficiencies in Aquestive Anaphylm Review, Approval Pending","url":"https://stock-news.laohu8.com/highlight/detail?id=2602988378","media":"Reuters","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2602988378?lang=en_us&edition=fundamental","pubTime":"2026-01-09 20:00","pubTimestamp":1767960048,"startTime":"0","endTime":"0","summary":"Aquestive Therapeutics Inc. announced that the U.S. Food and Drug Administration  has identified deficiencies in the company's New Drug Application  for Anaphylm , which currently preclude discussions of product labeling and post-marketing commitments. While the FDA's notification did not specify the deficiencies, the agency clarified that its review of the application is ongoing and no final decision has been made. Meanwhile, Aquestive is pursuing regulatory submissions for Anaphylm in Canada, Europe, and the United Kingdom, with plans to submit to Health Canada in the first half of 2026 and to the European Medicines Agency in the second half of 2026. The EMA has indicated that no further clinical trials are required prior to submission.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be inte","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260109:nNDL3CWB9h:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4585","LU2095319765.USD","BK4588","IE00BGHQF748.EUR","SG9999014021.USD","NDAQ","SG9999014039.USD","LU2210150020.SGD","LU0314104364.USD","BK4007","BK4112","IE00BKPKM429.USD","IE00B64PRP62.GBP","SG9999014005.SGD","LU2210149790.SGD","SG9999014013.SGD","IE00B3QW5Z07.USD","AQST"],"gpt_icon":0},{"id":"2602378987","title":"Aquestive Therapeutics Expands Global Regulatory Efforts for Anaphylm","url":"https://stock-news.laohu8.com/highlight/detail?id=2602378987","media":"Reuters","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2602378987?lang=en_us&edition=fundamental","pubTime":"2026-01-09 20:00","pubTimestamp":1767960020,"startTime":"0","endTime":"0","summary":"Aquestive Therapeutics Inc. is advancing its global expansion strategy for Anaphylm, its non-invasive epinephrine therapy for severe allergic reactions. The company has initiated regulatory engagements in Canada, Europe, and the United Kingdom, with plans to submit a New Drug Submission to Health Canada in the first half of 2026 and a marketing authorization application in Europe in the second half of 2026. Aquestive is also awaiting feedback from the UK's Medicines and Healthcare Products Regulatory Agency in early 2026. These efforts aim to expand access to Anaphylm internationally. Additionally, the company plans to hire a U.S. sales force following potential FDA approval.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. 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