Precigen Inc. provided an update on the commercialization of PAPZIMEOS at the 44th Annual J.P. Morgan Healthcare Conference. During their presentation, the company highlighted the rapid adoption and expanding market coverage of PAPZIMEOS, the first and only FDA-approved therapy for adults with recurrent respiratory papillomatosis (RRP). Company executives reported strong momentum in patient enrollment, widespread insurance coverage, and established manufacturing capabilities to meet growing demand. The event also showcased the company’s progress toward global expansion, including the validation of PAPZIMEOS’s Marketing Authorization Application by the European Medicines Agency.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Precigen Inc. published the original content used to generate this news brief on January 12, 2026, and is solely responsible for the information contained therein.
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