Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
T-773 is a small molecule radioligand developed as a positron emission tomography (PET) imaging agent targeting phosphodiesterase 10A (PDE10A). It acts as a highly selective and high-affinity inhibitor of PDE10A, an enzyme predominantly expressed in striatal medium spiny neurons. By binding to PDE10A, T-773 enables visualization and quantification of this enzyme in the brain using PET imaging. The compound has demonstrated strong selectivity for PDE10A over other phosphodiesterases and accumulates selectively in the striatum during preclinical studies. Its primary use is as a diagnostic radiopharmaceutical for research into neurological disorders such as schizophrenia and Huntington's disease[3][4]. T-773 was initially developed by Takeda Pharmaceutical.
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 T-773.