Market PotentialMarket metrics appear extremely attractive with existing apomorphine drug/device combination products priced high, providing benchmarks for SER-252 pricing if approved.
Product DevelopmentSerina has announced a new once-weekly injectable asset in development for tardive dyskinesia, highlighting its POZ platform potential.
Regulatory ApprovalThe FDA's feedback supports the design of the trial under the 505(b)(2) NDA pathway, which could fast-track SER-252's regulatory path by allowing the company to use existing knowledge of apomorphine.