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RecruitingNCT07321678

A Study to Evaluate the Efficacy, Safety, and Tolerability of ASC30 Tablets in Participants With Type 2 Diabetes Mellitus

A Phase II, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of ASC30 Tablets in Participants With Type 2 Diabetes Mellitus

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Ascletis Pharma (China) Co., Limited · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This randomized, double-blind, placebo-controlled Phase II study is designed to evaluate the efficacy, safety, and tolerability of ASC30 oral tablets formulation in participants with Type 2 Diabetes Mellitus

Conditions

Interventions

TypeNameDescription
DRUGASC30 tabletsASC30 tablets administered orally once daily
DRUGPlaceboPlacebo administered orally once daily

Timeline

Start date
2026-01-01
Primary completion
2026-08-01
Completion
2026-08-01
First posted
2026-01-07
Last updated
2026-01-07

Locations

8 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07321678. Inclusion in this directory is not an endorsement.

A Study to Evaluate the Efficacy, Safety, and Tolerability of ASC30 Tablets in Participants With Type 2 Diabetes Mellitu (NCT07321678) · Clinical Trials Directory