{"id":53389,"date":"2025-12-05T13:57:12","date_gmt":"2025-12-05T12:57:12","guid":{"rendered":"https:\/\/www.maiwald.eu\/?post_type=presseberichte&p=53389"},"modified":"2025-12-05T13:57:12","modified_gmt":"2025-12-05T12:57:12","slug":"royalty-pharma-and-denali-therapeutics-announce-275-million-royalty-funding-agreement","status":"publish","type":"presseberichte","link":"https:\/\/www.maiwald.eu\/jp\/press-coverage\/royalty-pharma-and-denali-therapeutics-announce-275-million-royalty-funding-agreement\/","title":{"rendered":"Royalty Pharma and Denali Therapeutics Announce $275 Million Royalty Funding Agreement."},"content":{"rendered":"\n


Royalty Pharma and Denali have entered into a $275 million financing agreement which, pursuant to a synthetic royalty agreement, is based on future net sales of tividenofusp alfa. Tividenofusp alfa is Denali\u2019s lead investigational TransportVehicle\u2122-enabled enzyme replacement therapy for the treatment of mucopolysaccharidosis type II (MPS II, Hunter syndrome). A Biologics License Application (BLA) for accelerated approval is currently under review by the U.S. Food and Drug Administration (FDA); the Prescription Drug User Fee Act (PDUFA) target date is April 5, 2026.<\/p>\n\n\n\n

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