Aquestive Therapeutics reports Q3 EPS (14c), consensus (11c)

Reports Q3 revenue $12.81M, consensus $12.94M. “The third quarter was another period of strong execution for Aquestive as we move closer to the launch of Anaphylm, if approved by the FDA,” said Daniel Barber, Chief Executive Officer of Aquestive. “The FDA’s decision not to convene an Advisory Committee further advances our regulatory path, and our NDA remains on track for the scheduled January 31, 2026 PDUFA goal date. We are fully engaged in U.S. launch preparations, continuing to build commercial readiness across distribution, medical affairs, and marketing channels, while also advancing regulatory discussions in Canada and the EU. Following our recently completed equity financing and strategic funding commitments, we believe we are well positioned to deliver on our mission to make epinephrine emergency treatment more accessible, portable, and patient-friendly. Finally, we remain committed to developing additional products from our AdrenaVerse(TM) epinephrine prodrug platform.”