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Minoxidil 5% / Botanical Hair Regimen in Men With Thinning Hair and Male Pattern Hair Loss/Androgenic Alopecia

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Galderma

Status

Completed

Conditions

Male Pattern of Hair Loss, Androgenic Alopecia

Treatments

Drug: Treatment: Minoxidil 5% / Botanical Hair Solution for Men

Study type

Interventional

Funder types

Industry

Identifiers

NCT02460289
GLI.04.SPR.US 10329

Details and patient eligibility

About

The purpose of this study is to characterize the effect of Minoxidil 5% Foam and Botanical Hair Solution Regimen in men with thinning hair and male pattern hair loss/androgenic alopecia (Norwood III & IV).

Enrollment

63 patients

Sex

Male

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Key Inclusion Criteria:

  1. Male patients age 18 to 60 years at the time of enrollment.
  2. Men who have self-perceived thinning hair.
  3. Men who have presentation of male pattern hair loss/androgenic alopecia (Norwood III & IV).

Key Exclusion Criteria:

  1. History of allergic reactions or severe intolerance to minoxidil and Botanical Hair Solution product ingredients.
  2. Plan to use any other concomitant therapy to treat hair loss, regrowth or volume during the study.

3 Subjects taking or planning to take topical or systemic prescription or OTC medications for treating hair loss and/or hair volume.

  1. Any significant history of concurrent medical disease, which in the judgment of the Investigator, would make the subject inappropriate for entry to this study including history of skin disease that may confound study results.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

63 participants in 1 patient group

Treatment
Experimental group
Treatment:
Drug: Treatment: Minoxidil 5% / Botanical Hair Solution for Men

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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