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» GC Biopharma and Hanmi’s once-monthly subcutaneous treatment for Fabry disease gains US IND clearance
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Endocrine/metabolic
GC Biopharma and Hanmi’s once-monthly subcutaneous treatment for Fabry disease gains US IND clearance
Sep. 3, 2024
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The FDA has cleared an IND for a phase I/II trial of LA-GLA (GC-1134A, HM-15421), an innovative enzyme replacement therapy for Fabry disease being co-developed by GC Biopharma Corp. and Hanmi Pharmaceutical Co. Ltd.
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Regulatory
Endocrine/metabolic
FDA
IND