Enregistrement de source primaire
La société a annoncé des résultats positifs de son étude de validation des facteurs humains et de son étude pharmacocinétique pour le film sublingual Anaphylm. Ces données soutiennent le resoumission prévu de la NDA à la FDA pour le traitement des réactions allergiques de type 1, y compris l'anaphylaxie.
aqst-20260810 0001398733 false 0001398733 2026-08-10 2026-08-10 UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, DC 20549 FORM 8-K CURRENT REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 Date of Report (Date of earliest event reported): August 10, 2026 Aquestive Therapeutics, Inc. (Exact name of Registrant as specified in its charter) Delaware 001-38599 82-3827296 (State or other jurisdiction of incorporation) (Commission File Number) (I.R.S. Employer Identification No.) 30 Technology Drive Warren , NJ 07059 ( 908 ) 941-1900 (Address, Including Zip Code, and Telephone Number, Including Area Code, of Registrant’s Principal Executive Offices) Not Applicable (Former name or former address, if changed since last report) ______________________
Aquestive : deux nouveaux brevets prolongent la protection d'Anaphylm jusqu'en 2037