drugset / Trial / NCT06481475

A Study to Investigate the Safety and Efficacy of YY003 in Adults With Moderate to Severe Glabellar Lines

NCT06481475 ↗

Phase 2 Completed 149 enrolled Chongqing Claruvis Pharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study is a two-part (Part A and Part B) randomized double-blind vehicle-controlled multi-center study in a total of 174 participants with moderate to severe glabellar lines. The objective of this study is to test the safety, efficacy, immunogenicity of YY003, and compare to vehicel control, in improving the appearance of moderate to severe glabellar lines.

Timeline

Start
2025-01-09
Primary completion
2025-10-22
Completion
2025-12-28

Drugs

EvaluationDrugModalityDoseRoute
Subject YY003 Protein / enzyme biologic — Intramuscular

Indications

No indication recorded.