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BioMarin has entered into an exclusive worldwide (ex-Korea) license agreement with GC Biopharma & Hanmi Pharm to develop & commercialize HM15421/GC1134A, an investigational long-acting SC enzyme replacement therapy for Fabry disease
GC & Hanmi will receive $70M upfront and are jointly eligible for up to $405M in development & commercial milestones, plus tiered royalties on net sales; GC & Hanmi retain commercialization rights in Korea
HM15421/GC1134A, a human recombinant α-Gal A enzyme therapy, is being evaluated in a P-I/II trial; following the study, BioMarin will lead all further development, manufacturing & commercialization; it received the US FDA’s ODD in 2024
Ref: PR Newswire | Image: BioMarin | Press Release
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The post BioMarin Licenses GC Biopharma and Hanmi Pharm’s HM15421/GC1134A for Fabry Disease in a ~$475M Deal appeared first on PharmaShots.
BioMarin Licenses GC Biopharma and Hanmi Pharm’s HM15421/GC1134A for Fabry Disease in a ~$475M Deal | PharmaVoice