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-0.0198252539140463 -0.0198252539140463 0.0118862819887347 -0.0508715128398457 -0.0508715128398457 -0.15288064931033 -0.117399210537987 -0.161751009003415
Stock impact report

Taysha Gene Therapies Reports Third Quarter 2024 Financial Results and Provides Corporate Update

Taysha Gene Therapies, Inc. (TSHA) 
Company Research Source: GlobeNewswire
High dose TSHA-102 was generally well tolerated with no SAEs or DLTs in two adolescent/adult patients and one pediatric patient as of data cutoff; IDMC approved continued enrollment in cohort two (high dose) across both REVEAL trials; eight patients dosed to date (low dose=4, high dose=4) Advanced discussions with the FDA on trial design, endpoints and potential use of established natural history dataset for Part B of REVEAL trials, and aligned on a meeting cadence to expedite the development plan for TSHA-102 following initial RMAT Type B meeting FDA approved use of pivotal TSHA-102 product in REVEAL trials based on successful demonstration of analytical comparability; Company released pivotal product manufactured with the final commercial manufacturing process following Type D CMC meeting Clinical data from cohort two (high dose) and cohort one (low dose) of both REVEAL trials expected in H1 2025    Conference call and live webcast today at 4:30 PM Eastern Time DALLAS, Nov. 13 Show less Read more
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