Aquestive Therapeutics to Present at 2026 ACAAI Annual Meeting
Aquestive Therapeutics announced that it will feature multiple oral and poster presentations at the 2026 American College of Allergy, Asthma, and Immunology (ACAAI) Annual Meeting.
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Aquestive Therapeutics Q3 2026 Earnings Call Transcript
Aquestive Therapeutics (NASDAQ:AQST) reported third-quarter financial results on Wednesday. The transcript from the company’s third-quarter earnings call has been provided below.Benzinga APIs provide real-time access to
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Aquestive Therapeutics Reports Third Quarter 2026 Financial Results
Aquestive Therapeutics announced its financial results for the third quarter ended September 30, 2026, reporting a decrease in total revenues to $7.6 million.
Aquestive Therapeutics to Report Third Quarter 2026 Financial Results on November 3
Aquestive Therapeutics announced it will release its financial results for the third quarter ended September 30, 2026, after market close on November 3, 2026, followed by an investor conference call on November 4.
8-K filing — Aquestive Therapeutics, Inc. (AQST)
Filed: 2026-10-19 AccNo: 0001398733-26-000063 Size: 6 MB Item 5.03: Amendments to Articles of Incorporation or Bylaws; Change in Fiscal Year Item 9.01: Financial Statements and Exhibits
FDA Accepts Aquestive Therapeutics’ Anaphylm NDA Resubmission; PDUFA Goal Action Date Set For March 16, 2027
FDA accepted the resubmission as complete and classified it as a Class 2 responsePrescription Drug User Fee Act (PDUFA) goal action date set for March 16, 2027Ex-U.S. strategy remains on track with Canadian NDS planned
Aquestive Therapeutics Announces FDA Acceptance of Anaphylm™ NDA Resubmission and PDUFA Goal Date of March 16, 2027
Aquestive Therapeutics announced that the FDA has accepted its resubmission of the New Drug Application (NDA) for Anaphylm™ (dibutepinephrine) sublingual film for treating Type I allergic reactions and anaphylaxis. The FDA assigned a PDUFA goal date of March 16, 2027, classified as a Class 2 response. If approved, Anaphylm would be the first and only oral rescue medication for severe allergic reactions. The company is also advancing its Canadian regulatory submission planned for Q4 2026.