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Regulatory

31 January 2017

GenSight Biologics receives FDA Orphan Drug Designation for GS030 in Retinitis Pigmentosa

08 September 2016

GenSight Biologics receives approval to include teenage patients in RESCUE and REVERSE Phase III trials with GS010 in Leber’s Hereditary Optic Neuropathy

01 September 2016

GenSight Biologics receives Orphan Drug Designation and Advanced Therapy Medicinal Product classification in Europe for GS030 in Retinitis Pigmentosa

10 September 2015

GenSight Biologics Receives IND Acceptance from FDA to Enter Phase III with GS010

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