Clinical DevelopmentSER-252 will advance into and through clinical development, achieving comparable efficacy to currently approved infusion systems with improved tolerability and ease of use in advanced Parkinson's Disease patients.
Pipeline ExpansionSerina has announced a new once-weekly injectable asset in development for tardive dyskinesia, highlighting its POZ platform potential.
Regulatory PathwayThe 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.