Efficacy and Safety of APSMNF in the Treatment of Male Androgenetic Alopecia
NCT07516561 · Status: NOT_YET_RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 336
Last updated 2026-04-13
Summary
The purpose of this study is to evaluate the efficacy and safety of APSMNF in the treatment of male androgenetic alopecia.
Conditions
- Alopecia, Androgenetic
Interventions
- DRUG
-
APSMNF 1
Administer twice a day during 24 weeks.
- DRUG
-
APSMNF 2
Administer twice a day during 24 weeks.
- DRUG
-
Eniagor®
Administer twice a day during 24 weeks.
Sponsors & Collaborators
-
Apsen Farmaceutica S.A.
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 60 Years
- Sex
- MALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-07-07
- Primary Completion
- 2029-08-02
- Completion
- 2029-08-02
Countries
- Brazil
Study Locations
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