Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
LV232 is a small molecule drug developed by Suzhou Vigonvita Life Sciences for the treatment of major depressive disorder (MDD). It is currently in Phase 2 clinical trials, with its primary therapeutic area being nervous system diseases, specifically depressive disorders. A Phase 1 exploratory study using positron emission tomography (PET) investigated LV232’s occupancy of the serotonin transporter (5-HTT) in the human brain after oral administration, suggesting that its antidepressant effect may be mediated through modulation or inhibition of the serotonin transporter. The drug is administered orally and has undergone multiple ascending dose and food-effect studies to evaluate safety, tolerability, and pharmacokinetics in healthy volunteers.
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 LV232.