drugset / Trial / NCT07002905

A Study to Evaluate the Efficacy, Safety, and Tolerability in Participants With Obesity or Overweight With Weight-Related Comorbidities

NCT07002905 ↗

Phase 2 Completed 125 enrolled Ascletis Pharma Inc
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This randomized, double-blind, placebo-controlled phase IIa study is designed to evaluate the efficacy, safety, and tolerability of ASC30 Tablets and ASC30 Tablets A1.

Timeline

Start
2025-07-03
Primary completion
2025-12-08
Completion
2025-12-08

Drugs

EvaluationDrugModalityDoseRoute
Subject ASC30 Unknown — Oral
Subject ASC30 tablets or ASC30 tablets A1 or placebo Unknown — Oral

Indications

No indication recorded.