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Sangamo Therapeutics Receives U.S. FDA Fast Track Designation for Isaralgagene Civaparvovec for the Treatment of Fabry Disease

Sangamo Therapeutics, Inc. , a genomic medicine company, today announced that the U.S. Food and Drug Administration has granted Fast Track Designation to isaralgagene civaparvovec, or ST-920, a... | May 22, 2023
Nathalie Dubois Stringfellow Sangamo Therapeutics Inc Development Officer Drug Administration European Medicines Agency Sangamo Therapeutics

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FDA Approves First Topical Gene Therapy for Treatment of Wounds in Patients with Dystrophic Epidermolysis Bullosa

FDA approves Vyjuvek, a herpes-simplex virus type 1 vector-based gene therapy, for the treatment of wounds in patients 6 months of age and older with dystrophic epidermolysis bullosa with mutation(s) in the collagen type VII alpha 1 chain gene.
Peter Marks Human Services Drug Administration Us Department Of Health Krystal Biotech Inc For Immediate Release
Source: fda.gov

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