Primärquellen-Eintrag
Das Unternehmen gab positive Ergebnisse seiner Human-Factors-Validierungsstudie und pharmakokinetischen Studie zu Anaphylm-Sublingualfilm bekannt. Diese Daten unterstützen die geplante erneute Einreichung des NDA bei der FDA zur Behandlung von Typ-1-Allergien, einschließlich 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: Zwei neue Patente verlängern den Anaphylm-Schutz bis 2037