Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07469085

A Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SV003 in Healthy Participants.

A Randomized, Double-blind, Placebo-controlled, Single-ascending-dose Phase I Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SV003 in Healthy Participants.

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Shanghai Synvida Biotechnology Co.,Ltd. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The objective of this clinical study is to evaluate the safety, tolerability, pharmacokinetic, and pharmacodynamic profiles of SV003 in healthy subjects.

Conditions

Interventions

TypeNameDescription
DRUGSV003SV003:Single-dose
DRUGPlaceboPlacebo : Single-dose

Timeline

Start date
2026-04-04
Primary completion
2026-10-31
Completion
2027-03-31
First posted
2026-03-13
Last updated
2026-04-08

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07469085. Inclusion in this directory is not an endorsement.