Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
TSHA-107 is an experimental gene therapy developed for the treatment of an autism spectrum disorder. It is designed as a gene transfer drug, implying the use of gene therapy techniques to address pathological mechanisms underlying the disease. TSHA-107 was initially developed by The University of Texas Southwestern Medical Center. Detailed mechanism of action and targeted gene(s) have not been publicly disclosed, but TSHA-107 belongs to the class of gene therapies intended to introduce functional genetic material into cells to correct or mitigate disease processes[5][13].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on TSHA-107.