Overview
This is a multi-centers, randomized, double-blind, parallel-group, Phase 2 Trial to evaluate the efficacy and safety of CKD-498 in female patients with Androgenetic Alopecia
Description
Participants were randomly assigned in a 1:1:1:1 ratio to the following group: 3 dose of CKD-498 and Placebo. The patients are prescribed oral administration of the appropriate IP daily (3 tablets: actual medication and placebo) for 24 weeks.
Eligibility
Key Inclusion Criteria:
- Female of age 19-54 years
- Clinical Diagnosis of Androgenetic Alopecia
- Written informed consent
Key Exclusion Criteria:
- Other types of Alopecia or other diseases that can cause hair loss
- Clinically significant scalp disease such as seborrheic dermatitis or psoriasis
- Clinically significant hepatic disease, thyroid disease, or mental illness, as determined by the Investigator
- Women who are pregnant or breastfeeding
- Women of childbearing potential who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study period and for up to 4 weeks after the last dose of study drug