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RecruitingNCT07289464

A Clinical Study of RSS0343 in Healthy Subjects

A Randomized, Double-blind, Placebo-controlled Phase I Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetics of RSS0343 Following Multiple Oral Doses in Healthy Subjects, as Well as Its Effects on the QT/QTc Interval

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
48 (estimated)
Sponsor
Reistone Biopharma Company Limited · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

This is a phase I study to evaluate the safety, tolerability and pharmacokinetics of RSS0343 following multiple oral doses in healthy subjects, as well as its effects on the QT/QTc interval.

Conditions

Interventions

TypeNameDescription
DRUGRSS0343 TabletsRSS0343 tablets, oral.
DRUGRSS0343 Tablets PlaceboRSS0343 tablets placebo, oral.

Timeline

Start date
2026-01-04
Primary completion
2026-09-01
Completion
2026-09-01
First posted
2025-12-17
Last updated
2026-01-14

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07289464. Inclusion in this directory is not an endorsement.

A Clinical Study of RSS0343 in Healthy Subjects (NCT07289464) · Clinical Trials Directory