A Phase 2 Clinical Study of CU-20401

PHASE2CompletedINTERVENTIONAL
Enrollment

108

Participants

Timeline

Start Date

December 20, 2023

Primary Completion Date

September 2, 2024

Study Completion Date

September 2, 2024

Conditions
Efficacy and Safety
Interventions
DRUG

Subcutaneous injection of CU-20401

Reconstitute the product with 0.9% sodium chloride solution for injection, respectively, before use, for a single subcutaneous injection in the submental fat area.

Trial Locations (1)

430000

Union Hospital Tongji Medical College Huazhong University of Science and Technology, Wuhan

All Listed Sponsors
lead

Cutia Therapeutics(Wuxi)Co.,Ltd

INDUSTRY

NCT06194188 - A Phase 2 Clinical Study of CU-20401 | Biotech Hunter | Biotech Hunter