Aquestive Therapeutics demonstrated strong momentum heading into its Q3 2025 earnings, highlighted by increased awareness of its Anaphylm dibutepinephrine Sublingual Film program and preparations for a potential FDA approval.
- Nearly 25% of allergists have engaged with Aquestive's CME training, enhancing awareness of Anaphylm ahead of the FDA review due by January 31, 2026.
- Strategic prelaunch activities for Anaphylm are on track, with marketing materials finalized and a supply chain ready for rapid production upon FDA approval.
- Leadership restructuring aims to bolster efforts in both the Anaphylm launch and the Adrenaverse platform, including the appointment of Dr. Matthew Davis as Chief Development Officer.
- The company anticipates initiating clinical trials for its AQST-108 program in January 2026, further expanding its product pipeline.
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