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Taysha Gene Therapies Announces Initiation of Clinical Development of TSHA-102 in Rett Syndrome | DNA RNA and Cells

Taysha Gene Therapies Announces Initiation of Clinical Development of TSHA-102 in Rett Syndrome

United statesUniversity hospitalSarah sinnettSuyash prasadSteven grayElsa rossignolHead of researchGood laboratory practicesI taysha gene therapies incChild university hospitalDevelopment of tayshaEuropean commissionDrug administrationInternational rett syndrome foundationUt southwestern medical centerRett syndrome research

Taysha Gene Therapies, Inc : Taysha Receives Orphan Drug Designation from the European Commission for TSHA-102 for the Treatment of Rett Syndrome

Taysha Gene Therapies, Inc : Taysha Receives Orphan Drug Designation from the European Commission for TSHA-102 for the Treatment of Rett Syndrome
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United statesKimberly leeCarolyn hawleyCompany contactEuropean commissionCanale communicationsDrug administrationExchange commissionTaysha gene therapies incEuropean unionCorporate communicationsUt southwestern gene therapy programGene therapiesChief executive officerResponsive auto regulatory elementGene therapy program