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Rogaine (minoxidil)
Potassium channel opener that stimulates hair follicles (topical) or causes arteriolar vasodilation (oral) for hair loss and severe hypertension.
Minoxidil (Rogaine) is the first FDA-approved topical treatment for hair loss, discovered serendipitously from its antihypertensive use. Available OTC as topical solution/foam. Available generically.
At a glance
| Generic name | minoxidil |
|---|---|
| Also known as | Rogaine, Regaine, Loniten (oral) |
| Sponsor | Generic (originally Upjohn/Pfizer) |
| Drug class | Vasodilator (potassium channel opener), Hair growth stimulant |
| Target | ATP-sensitive inward rectifier potassium channel 1, Sulfonylurea receptor 2, Kir6.2 |
| Modality | Small molecule |
| Therapeutic area | Cardiovascular |
| Phase | FDA-approved |
| First approval | 1988-08-18 (United States) |
Mechanism of action
Minoxidil was originally developed as an oral antihypertensive but hair growth was noticed as a side effect. The topical formulation (Rogaine) became the first FDA-approved treatment for androgenetic alopecia. It prolongs the anagen (growth) phase of hair follicles and increases follicular size. The oral form is reserved for severe refractory hypertension.
Approved indications
- Alopecia
- Hypertensive disorder
Common side effects
Key clinical trials
- International Phase III, Multi Center, Randomized, Double Blind, Placebo and Active Controlled and Parallel Group Clinical Trial to Evaluate the Efficacy and Safety of Oral Minoxidil 1 mg in Female Pa (Phase 3)
- A Multicenter, Randomized, Double-Blind, Placebo-Controlled Clinical Study on the Efficacy and Safety of 5% Minoxidil Foam in the Treatment of Female Androgenetic Alopecia (Phase 3)
- A Randomized Controlled Trial Comparing Platelet Rich Plasma (PRP) to Minoxidil Foam for Treatment of Androgenic Alopecia in Women (Phase 1)
- A Prospective Multicentric Open Label Randomized Bio-Interventional Phase I/II Pilot Study To Evaluate The Safety And Efficacy Of Autologous Human Platelet Lysate (HPL) For Treatment Of Androgenetic A (Phase 1)
- A Multicenter, Randomized, Double-blind, Placebo-controlled Phase II Clinical Trial to Evaluate the Efficacy and Safety of CG2001 in Chinese Adult Male Participants With Androgenetic Alopecia (Phase 2)
- Randomised, Crossover Bioavailability Clinical Trial of Oral Minoxidil 1 MG, After Single and Multiple Dose Administration to Healthy Volunteers Under Fasting Conditions. (Phase 1)
- Scientific Evaluation of the Safety and Efficacy of Herbal and Non Herbal Formulations in Mitigating Hair Fall, Promoting Hair Growth, and Preventing Premature Hair Graying. (NA)
- Phase I Study of Safety and Pharmacokinetics of Once-Daily Topical Solution in Male Subjects With Androgenetic Alopecia (Phase 1)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| FDA label | Mechanism, indications, dosing, boxed warnings, drug interactions |
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |