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BioMarin Pharmaceutical Enters License Agreement With GC Biopharma And Hanmi Pharm To Develop And Commercialize Its HM15421/GC1134A Investigational Long-Acting Enzyme Replacement Therapy For Fabry Disease; Company To Pay $70M Up Front, With Partners Eligible For Up To $405M In Milestones

Oct 29, 2026 · 08:52 AM ET· updated 1h ago

HM15421/GC1134A is a human recombinant alpha-galactosidase A (a-Gal A) enzyme therapy currently being studied in a Phase 1/2 clinical trial in people living with Fabry disease and has the potential to be the first

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Why It Matters

BioMarin paid $70 million upfront to partner with two Korean companies to develop a new Fabry disease treatment. This shows the company is betting on new medicines and sharing costs and risks with other teams.

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Source: Benzinga · Read the original report at the publisher. Headline and figures shown for context; data may be delayed.

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