Trial intelligence / Profile preview

VV913 Multiple Ascending Dose Study in Healthy Chinese Participants

NCT07507838Phase 1Recruiting

Sponsor
Vigonvita Life Sciences
Start
Apr 2026
Primary completion
Dec 2026
Modality
Small Molecules
Countries
1
01

Overview

Phase 1, randomised, double-blind trial of VV913 (4 arms), sponsored by Vigonvita Life Sciences. Primary endpoints: Incidence of Treatment-Emergent Adverse Events at 6 days, Maximum Observed Plasma Concentration at 72 hours and 9 more. Started Apr 2026; status: recruiting.

02

Drugs

VV913

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