Taysha Gene Therapies reported a net loss of $50.1 million for the first quarter of 2022. Research and development expenses were $37.8 million, and general and administrative expenses were $11.5 million. As of March 31, 2022, the company had $96.6 million in cash and cash equivalents.
Initiated clinical development of TSHA-102 for Rett Syndrome under recently approved Clinical Trial Application (CTA) with preliminary Phase 1/2 data expected by year-end 2022.
Received Orphan Drug Designation from the European Commission for TSHA-120 for giant axonal neuropathy (GAN).
Completed commercially representative GMP batch for TSHA-120; regulatory update expected in mid-2022.
Existing cash and cash equivalents, along with full access to the term loan facility, is expected to fund operating expenses and capital requirements into the fourth quarter of 2023.
Taysha Gene Therapies anticipates a regulatory update for TSHA-120 in GAN by mid-2022 and preliminary clinical data from the REVEAL study for TSHA-102 in Rett syndrome by year-end 2022.