Treatment of Androgenetic Alopecia in Men for 24 Weeks

NCT04721548 | Completed Phase 3

• 1 other identifier: EF171
• Study Type: interventional
• Target: 336
• Locations: 1 country
• Sites: 1

Brief Summary

A prospective, randomized, double-blind, single-center, placebo-Controlled, parallel-group study to evaluate the efficacy and safety of a new pharmaceutical form Minoxidil 5% in men after 24 weeks of treatment. ⚠️Study will only be conducted in research centers in Brazil (please do not send e-mail if your center is outside brazil).

Conditions

Alopecia

Outcome Measures

Primary Outcomes (1)

• Absolute change in terminal thread density in the target area determined 180 (±3) days after the start of treatment compared to baseline density.

  The density of terminal hairs will be evaluated by phototrichogram (FotoFinder leviacam® and Trichoscale Al® Dermatoscope), with the baseline density resulting from the images captured on the VR and VR+2 days visits and the final density resulting from the images captured on the V5 and V5+2 days visits. Terminal wires will be classified as those with diameter greater than or equal to 30 um.

  24 weeks

Study Arms (2)

Minoxidil´s Placebo

PLACEBO COMPARATOR

The recommended dosage is 1 ml of the solution twice a day (morning and evening).

Drug: Placebo

Topical Minoxidil 5%

EXPERIMENTAL

The recommended dosage is 1 ml of the solution twice a day (morning and evening).

Drug: Minoxidil Topical Foam

Interventions

Minoxidil Topical Foam DRUG

Apply 1 mL of solution twice a day.

Topical Minoxidil 5%

Placebo DRUG

1 mL of solution twice a day.

Minoxidil´s Placebo

Eligibility Criteria

• Age: 18 Years - 65 Years
• Gender Eligibility Details: Male
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Age between 18 and 65 years;
• Male pattern baldness identified according the Norwood Hamilton scale: stage IIIv vertex, stage IV, or stage V;
• Terminal hair density equal to or less than 220 hairs/cm2 measured with the Trichoscale Al;
• Subjects who are willing and able to comply with all requirements of the study for the intended period;
• Subjects who give their consent to the study after thoroughly clarification and who personally signed and dated the informed consent document has been informed of all pertinent aspects of the trial;

You may not qualify if:

• Current or 6 months dated back use of:
• Minoxidil, finasteride, or any 5 alpha-reductase inhibitor;
• Medications that can potentiate Hypertrichosis, such as: cyclosporine, phenytoin, psolarenes, oral glucocorticoids (except inhalers), lithium, phenothiazinics
• Medications with anti-androgenic properties, such as: cyproterone, spironolactone, ketoconazole, flutamide, bicalutamide.
• Any anabolic steroid ;
• Current or 8 weeks dated back use of herbal products such as saw palmetto;
• Isotretinoin for at least 12 months;
• Current or 2 weeks dated back use of dietary or vitamin supplements;
• Subjects who had a dignosis of malignant disease in the alopecia area in the period of 05 years;

Sponsors & Collaborators

• Eurofarma Laboratorios S.A.: lead

Study Sites (1)

Eurofarma Laboratorios S.A

São Paulo, São Paulo, 06696-000, Brazil

Location

MeSH Terms

Conditions

Alopecia

Condition Hierarchy (Ancestors)

Hypotrichosis; Hair Diseases; Skin Diseases; Skin and Connective Tissue Diseases; Pathological Conditions, Anatomical; Pathological Conditions, Signs and Symptoms

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, INVESTIGATOR
• Masking Details: Masking will be adopted in this study, in which the experimental products under evaluation will be provided in a masked way, that is, one group will receive an experimental drug (Minoxidil 5%) and another group will receive a placebo (product without the active ingredient) in identical primary and secondary packaging to avoid potential bias, so neither the researcher nor the research participant will know what is being applied.
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: Participants will be randomized at a 2: 1 ratio to receive new pharmaceutical form Minoxidil 5% and placebo, respectively. The primary objective of the MINOX study is to demonstrate the superiority of a new topical 5% pharmaceutical form of minoxidil (experimental drug) in treating men with androgenetic alopecia (Hamilton-Norwood scale IIIv, IV or V) compared to placebo when administered for 180 days.

Study Record Dates

• First Submitted: January 14, 2021
• First Posted: January 22, 2021
• Study Start: March 2, 2023
• Primary Completion: March 6, 2024
• Study Completion: March 6, 2024
• Last Updated: February 17, 2025

Record last verified: 2025-02

Data Sharing

• IPD Sharing: Will not share

Locations

BR (1)