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Taysha and Catalent Expand Partnership for TSHA-102 Manufacturing Support

Taysha Gene Therapies logoTaysha Gene Therapies
Sig2.60Sen+4.47Env0.00Soc+2.42Gov+0.73

Rett syndrome progresses through early stagnation, regression, plateau and late motor deterioration, with MECP2 mutations affecting 15,000–20,000 patients in the U.S., EU and U.K. TSHA-102, Taysha’s AAV gene therapy candidate, targets the genetic root cause, where no approved disease-modifying options exist. Taysha and Catalent expand their strategic partnership to secure long-term commercial manufacturing capacity and scalable supply for TSHA-102 at Catalent’s nearly 40 global sites.

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