drugset / Trial / NCT07710326

Safety and Pharmacokinetics Study of Multiple Ascending Doses of VV261 Tablets

NCT07710326 ↗

Phase 1 Not yet recruiting 16 enrolled Vigonvita Life Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a randomized, double-blind, placebo-controlled, multiple ascending-dose study to evaluate the safety, tolerability and pharmacokinetics characteristics of VV261 tablets in healthy adults.

Timeline

Start
2026-08-01
Primary completion
2026-11-30
Completion
2026-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject VV261 Unknown 600 mg Oral
Subject VV261 Unknown 900 mg Oral

Indications

No indication recorded.