FDA
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GenSight Biologics Reports Cash Position as of March 31, 2024, and Provides Business Update
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GenSight Biologics Announces Successful Manufacture of LUMEVOQ® GMP Batch
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GenSight Biologics Reports Cash Position as of December 31, 2021, and Provides Operational Update
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GenSight Biologics Reports Topline Results from REFLECT Phase III Clinical Trial, Confirming LUMEVOQ® Efficacy Including Better Efficacy with Bilateral Treatment
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GenSight Biologics Reports New Analysis Demonstrating Statistically Significant and Clinically Meaningful Difference Between Visual Outcomes in LUMEVOQ®-Treated Patients and Natural History of Leber
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GenSight Biologics completes enrollment of GS010 REFLECT Phase III trial in the treatment of Leber Hereditary Optic Neuropathy ahead of schedule
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GenSight Biologics Receives FDA Orphan Drug Designation for GS030 in Retinitis Pigmentosa
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