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Taysha Gene Therapies, Inc. is promoting a webinar hosted by the Child Neurology Society featuring Dr. Arthur Partikian, a leading expert in Rett syndrome.
The session is set to explore how natural history research is shaping more patient-centered clinical trials, refining treatment expectations, and preparing the Rett syndrome community for emerging therapies. The event reflects a growing emphasis on integrating scientific insights with direct clinical application for rare disease communities.
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Earlier this year, Taysha Gene Therapies secured a commercial supply agreement with Catalent for TSHA-102, marking a step in advancing its pipeline through new manufacturing partnerships. The company’s shares rose 6.7% to $6.17 following the announcement of its upcoming second quarter 2026 earnings and corporate update earlier this month. These developments come as Taysha continues to engage clinical and patient communities in the rare disease space.