drugset / Trial / NCT06679959

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of ASC30 Injection in Participants With Obesity

NCT06679959 ↗

Phase 1/2 Completed 115 enrolled Ascletis Pharma Inc
RandomizedSequentialQuadruple-blindTreatment

Summary

This randomized, double-blind, placebo-controlled single ascending dose (SAD)/ multiple ascending dose (MAD) study is designed to evaluate the safety, tolerability, pharmacokinetics, and efficacy of ASC30 injection

Timeline

Start
2024-09-16
Primary completion
2026-03-26
Completion
2026-03-26

Drugs

EvaluationDrugModalityDoseRoute
Subject ASC30 Unknown — Subcutaneous

Indications

No indication recorded.