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Not Yet RecruitingNCT07507838

Safety and Pharmacokinetics Study of Multiple Ascending Doses of VV913 Capsules

Safety and Pharmacokinetics Study of Multiple Ascending Doses of VV913 Capsules in Chinese Healthy Participants

Status
Not Yet Recruiting
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
24 (estimated)
Sponsor
Vigonvita Life Sciences · Industry
Sex
Male
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This study is a single-center, randomized, double-blind, placebo-controlled, dose-escalation trial to assess the safety, tolerability, pharmacokinetics (PK) of multiple doses of VV913 in Chinese healthy adult participants.

Conditions

Interventions

TypeNameDescription
DRUGVV913 4mg group6 participants will receive VV913 4mg orally; 2 participants will receive placebo orally.
DRUGVV913 8mg group6 participants will receive VV913 8mg orally; 2 participants will receive placebo orally.
DRUGVV913 15mg group6 participants will receive VV913 15mg orally; 2 participants will receive placebo orally.

Timeline

Start date
2026-04-01
Primary completion
2026-12-31
Completion
2026-12-31
First posted
2026-04-02
Last updated
2026-04-02

Source: ClinicalTrials.gov record NCT07507838. Inclusion in this directory is not an endorsement.

Safety and Pharmacokinetics Study of Multiple Ascending Doses of VV913 Capsules (NCT07507838) · Clinical Trials Directory