Major Product Developments
Announced a new product candidate, AQST-108, for alopecia areata. Expanded Libervant launch in the 2- to 5-year-old demographic. Completed final adult study for Anaphylm and submitted pre-NDA briefing book to the FDA.
Anaphylm Clinical Study Success
OASIS study confirmed Anaphylm absorption profile remains unchanged with or without an allergen, demonstrating significant symptom resolution improvements.
Commercial Expansion and Market Access
Libervant achieved Medicaid coverage in all 50 states and agreements with two of the top three PBMs.
Revenue Growth
Total revenues increased by 4% to $13.5 million in Q3 2024, driven by license and royalty revenue.
Positive CMC Feedback from FDA
Received supportive responses from the FDA on the chemistry, manufacturing, and controls pre-NDA questions for Anaphylm.