Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07479641

A Bioequivalence Study of Two Formulations of HRS-1893 Tablets in Healthy Participants

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
36 (estimated)
Sponsor
Shandong Suncadia Medicine Co., Ltd. · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

This study will investigate the bioequivalence between two formulations of HRS-1893 tablets. Safety and tolerability will also be assessed.

Conditions

Interventions

TypeNameDescription
DRUGTest formulation of HRS-1893 tabletTest formulation of HRS-1893 tablet, oral.
DRUGReference formulation of HRS-1893 tabletReference formulation of HRS-1893 tablet, oral.

Timeline

Start date
2026-04-14
Primary completion
2026-06-01
Completion
2026-07-01
First posted
2026-03-18
Last updated
2026-04-17

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07479641. Inclusion in this directory is not an endorsement.

A Bioequivalence Study of Two Formulations of HRS-1893 Tablets in Healthy Participants (NCT07479641) · Clinical Trials Directory