A Phase 2 Study to Evaluate the Safety and Efficacy of CKD-498 in Female Patients With Androgenetic Alopecia

PHASE2CompletedINTERVENTIONAL
Enrollment

121

Participants

Timeline

Start Date

December 20, 2022

Primary Completion Date

December 15, 2023

Study Completion Date

December 15, 2023

Conditions
Androgenetic Alopecia
Interventions
DRUG

CKD-498 dose#1

oral, once daily, 24 weeks

DRUG

CKD-498 dose#2

oral, once daily, 24 weeks

DRUG

CKD-498 dose#3

oral, once daily, 24 weeks

DRUG

Placebo of CKD-498 dose#1

oral, once daily, 24 weeks

DRUG

Placebo of CKD-498 dose#2

oral, once daily, 24 weeks

DRUG

Placebo of CKD-498 dose#3

oral, once daily, 24 weeks

Trial Locations (1)

13620

Seoul National University Bundang Hospital, Gyeonggi-do

Sponsors
All Listed Sponsors
lead

Chong Kun Dang Pharmaceutical

INDUSTRY