Taysha Gene Therapies reported a net loss of $51.2 million for Q3 2021. The company made significant advances across multiple programs, including regulatory meetings and preclinical data publications.
Submitted an end-of-Phase meeting request for TSHA-120 with a major ex-US regulatory agency.
Expect to report clinical safety and functional MFM32 data for TSHA-120 from the high dose cohort in December.
Remain on track to report preliminary clinical safety data and Hex A enzyme activity for TSHA-101 in December.
Anticipate preliminary clinical data for the first-generation construct in CLN7 disease in December.
Taysha Gene Therapies anticipates several milestones across its programs and expects to provide updates throughout the remainder of the year.
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