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Antiandrogen comparison for hair loss

A side-by-side of the drugs, topicals and supplements that work on the androgen pathway, with who they were studied in and how strong the evidence is.

hair lossthinningreceding hairline

Key takeaways

  • Men: finasteride is the best-evidenced drug (large trials). Dutasteride lowers DHT more and beat finasteride 1 mg in head-to-head trials, but outside Korea and Japan it is off-label. Kaufman 1998; Gubelin Harcha 2014 See finasteride and dutasteride.
  • Women: finasteride 1 mg failed in postmenopausal women in a 1-year trial. Spironolactone is the most-used oral option, with trial support mainly as an add-on to minoxidil. Price 2000; Werachattawatchai 2025 See spironolactone.
  • Bicalutamide is a second-line option in women, and 2026 comparisons with spironolactone disagree: hair counts favoured bicalutamide, while a 24-month clinical-rating cohort favoured spironolactone. Jha 2026; Gil-Redondo 2026
  • Flutamide and cyproterone acetate have older, small, mixed trials and serious safety flags (liver failure; meningioma). Carmina 2003; Weill 2021
  • Topical antiandrogens are the 2026 story. Clascoterone 5% reported positive phase 3 results in 1,465 men (company data, filing planned early 2027); pyrilutamide reported a positive China pivotal result; GT20029 is earlier. A topical finasteride spray is already authorised in parts of the EU.
  • Supplements such as saw palmetto and pumpkin seed oil have small, short, mostly industry-linked trials. "5-alpha-reductase blocker" claims for beta-sitosterol or spearmint are not backed by hair data. Evron 2020
  • A Delphi consensus of 11 Canadian physicians recommended oral and topical finasteride, oral dutasteride, topical and oral minoxidil, PRP and microneedling, and listed flutamide as not recommended. Landells 2025

The three ways in

Pattern hair loss depends on testosterone being converted to DHT and on DHT acting on the follicle's androgen receptor. There are three ways in:

  1. Block the enzyme that makes DHT: finasteride, dutasteride, and weakly some botanicals.
  2. Block the receptor: spironolactone, bicalutamide, flutamide, cyproterone, clascoterone, pyrilutamide and RU58841.
  3. Destroy the receptor: GT20029.

The biology is in DHT and pattern hair loss.

Comparison table

Option Route Studied in Best evidence Approved for hair? Main safety flag
Finasteride oral 1 mg; topical spray exists men (no benefit in a postmenopausal-women trial) About 107 to 138 more hairs than placebo in a vertex circle at 1 to 2 years Kaufman 1998 Yes, men (US, EU, UK) Sexual and mood reports, EU/UK warnings, debated persistent symptoms; harms a male fetus
Dutasteride oral 0.5 mg; mesotherapy men 0.5 mg beat finasteride 1 mg in 917 men Gubelin Harcha 2014 Korea and Japan only Same warnings as finasteride, longer half-life
Spironolactone oral women Small trials as add-on to minoxidil, large case series No (off-label) High potassium, irregular periods, pregnancy; not for men
Bicalutamide oral 50 mg women One 204-woman trial, retrospective cohorts No Liver injury, pregnancy
Flutamide oral or topical women One small unmasked trial No Boxed warning: liver failure
Cyproterone acetate oral women Two trials, mixed No Dose-related meningioma; EMA restrictions
Oral contraceptives oral women Indirect, mostly acne and excess hair No Clots; meningioma with some progestogens
Clascoterone topical 5% men Two phase 3 trials, company-reported No (1% acne cream approved in the US) Reported similar to vehicle
Pyrilutamide topical men Company-reported China pivotal trial No Reported mild
GT20029 topical men 12-week phase 2 in 180 men No Reported mild
Alfatradiol topical women Slowed loss only, in one trial Germany Low
RU58841 topical none (animal) Graft and macaque data; human absorption shown in 2026 No (research chemical) Unknown
Fluridil topical men One 43-man inventor study Cosmetic in some markets Unknown
Saw palmetto oral or topical both Small trials; 38% vs 68% improved in an open comparison with finasteride Rossi 2012 No (supplement) Low
Pumpkin seed oil oral or topical both Two small trials No Low
Beta-sitosterol, spearmint oral none for hair Lab and hormone data only No Low
Creatine oral men One trial: no change in DHT or hair n/a n/a

Pipeline

  • A long-acting finasteride injection (IVL3001) has a 40-person pharmacokinetic study registered, and a topical minoxidil-finasteride foam (CG2001) has a 44-person phase 1 published in 2026. Li 2026; NCT04945226
  • The dutasteride injection CKD-843 (every 3 months) is in a 288-man Korean phase 3. NCT06916793

What it means for your hair

  • Men with early recession or crown thinning: the strongest evidence is for oral and topical finasteride and dutasteride. The EU product information says efficacy at the temples is not established, so keep expectations realistic.
  • Women who could become pregnant: any oral antiandrogen needs reliable contraception, and the choice differs by whether signs of hormone excess (acne, excess hair, irregular periods) are present. Ong 2025
  • Postmenopausal women: finasteride 1 mg did not help in a placebo-controlled trial, though higher-dose open studies exist; spironolactone and topicals are used. Price 2000
  • Coarse or tightly coiled hair and traction or scarring alopecia: pattern-loss data come mostly from lighter-skinned groups, and androgen-pathway drugs do not treat scarring or traction alopecia, so get a diagnosis first.

Myths and facts

  • Myth: you need high hormone levels to have pattern hair loss. Fact: in an 80-woman antiandrogen series no hormone level predicted who responded, and the follicle's own sensitivity and genetics matter. Sinclair 2005
  • Myth: natural DHT blockers equal finasteride. Fact: in the head-to-head open study, saw palmetto helped 38% vs 68% on finasteride. Rossi 2012
  • Myth: topical antiandrogens will replace pills now. Fact: none of the new topical agents is approved for hair as of 10 October 2026, and filings are planned for 2027 or later.

Bottom line

Match the option to sex, pregnancy plans and hormone signs, and leave prescription antiandrogens to a clinician. Most patterns also benefit from minoxidil, which works by a different pathway (see minoxidil). Judge response at 6 to 12 months using the same photos, because most studies above ran only 12 to 24 weeks. Discuss with a doctor.

Studies 16

Kaufman KD et al. Finasteride in the treatment of men with androgenetic alopecia. J Am Acad Dermatol. 1998

Design
rct
People
1,553
Duration
1 year plus 1-year blinded extension
Who
men 18-41 with vertex pattern hair loss

Tested: finasteride 1 mg/day vs placebo

Result: Finasteride grew about 107 more hairs than placebo at 1 year and about 138 more at 2 years in a 5.1 cm2 vertex circle (baseline about 876); placebo men kept losing hair.

Read the study ↗

Gubelin Harcha W et al. A randomized, active- and placebo-controlled study of the efficacy and safety of different doses of dutasteride versus placebo and finasteride in the treatment of male subjects with androgenetic alopecia. J Am Acad Dermatol. 2014

Design
rct
People
917
Duration
24 weeks
Who
men with androgenetic alopecia

Tested: dutasteride 0.02, 0.1 or 0.5 mg vs finasteride 1 mg vs placebo

Result: Dutasteride 0.5 mg beat finasteride 1 mg on hair count, hair width and frontal photos; adverse events were similar. GSK-funded.

Read the study ↗

Price VH et al. Lack of efficacy of finasteride in postmenopausal women with androgenetic alopecia. J Am Acad Dermatol. 2000

Design
rct
People
137
Duration
1 year
Who
postmenopausal women with androgenetic alopecia

Tested: finasteride 1 mg/day vs placebo

Result: No benefit over placebo on any endpoint.

Read the study ↗

Werachattawatchai P et al. Oral spironolactone for female pattern hair loss in premenopausal women: placebo-controlled pilot randomized controlled trial. Int J Womens Dermatol. 2025

Design
rct
People
48
Duration
24 weeks
Who
premenopausal women with female pattern hair loss, all on minoxidil 3%

Tested: spironolactone 100 mg vs placebo

Result: Moderate-to-marked improvement in 38% vs 9% (p = 0.034); terminal hairs +9.5 vs +5.3/cm2 (p = 0.063); menstrual irregularity 37.5%.

Read the study ↗

Jha AK et al. Spironolactone vs bicalutamide in female pattern hair loss: randomized clinical trial. Clin Exp Dermatol. 2026

Design
rct
People
204
Duration
24 weeks
Who
women with female pattern hair loss, single centre in India

Tested: bicalutamide 50 mg vs spironolactone 100 mg

Result: Frontal hair count rose 5.05 vs 3.13/cm2 favouring bicalutamide (p<0.001); vertex 6.32 vs 3.06; the authors found no significant difference in clinical endpoints; adverse events 11.7% vs 18.6%.

Read the study ↗

Gil-Redondo R et al. Spironolactone versus bicalutamide for female pattern hair loss: 24-month retrospective study. Dermatol Ther (Heidelb). 2026

Design
cohort
People
187
Duration
24 months
Who
women with female pattern hair loss, Madrid

Tested: spironolactone (128) vs bicalutamide (59)

Result: At least one grade of improvement in 54.4% on spironolactone vs 37.3% on bicalutamide (p = 0.030); more laboratory abnormalities with bicalutamide; spironolactone doses above 100 mg did best.

Read the study ↗
Show 10 more studies

Carmina E, Lobo RA. Treatment of hyperandrogenic alopecia in women. Fertil Steril. 2003

Design
rct
People
48
Duration
1 year
Who
premenopausal women with hyperandrogenic alopecia (randomised, unmasked)

Tested: flutamide 250 mg, cyproterone acetate 50 mg plus ethinyl estradiol, finasteride 5 mg, or no treatment

Result: Only flutamide moved the Ludwig score (21% reduction); the other treatments were not significant.

Read the study ↗

Weill A et al. High dose cyproterone acetate and intracranial meningioma: a cohort study of 253,777 women in France. BMJ. 2021

Design
cohort
People
253,777
Who
French women starting high-dose cyproterone acetate

Tested: cyproterone acetate

Result: Adjusted hazard ratio 6.6 (95% CI 4.0-11.1) for meningioma surgery or radiotherapy, 21.7 above 60 g cumulative dose.

Read the study ↗

Evron E et al. Saw palmetto, a systematic review in alopecia. Skin Appendage Disord. 2020

Design
systematic review
Who
patients with alopecia (5 RCTs and 2 cohorts)

Tested: saw palmetto-containing products, 100-320 mg

Result: Positive effects reported (for example density up in 83% of patients in one study); the authors say high-quality data are lacking and many products were blends.

Read the study ↗

Rossi A et al. Finasteride 1 mg daily administration vs Serenoa repens 320 mg in male androgenetic alopecia: two-year study. Int J Immunopathol Pharmacol. 2012

Design
rct
People
100
Duration
24 months
Who
men with mild-to-moderate androgenetic alopecia (open label)

Tested: Serenoa repens 320 mg/day vs finasteride 1 mg/day

Result: Hair growth increased in 38% on saw palmetto vs 68% on finasteride.

Read the study ↗

Landells I et al. A Canadian consensus on androgenetic alopecia. J Cutan Med Surg. 2025

Design
guideline
People
11
Who
11 Canadian physicians (Delphi consensus; some co-authors employed by L'Oreal Canada)

Tested: expert ratings of 17+ interventions

Result: Recommended oral and topical finasteride, oral dutasteride, minoxidil, PRP and microneedling; listed flutamide among interventions not recommended.

Read the study ↗

Sinclair R et al. Treatment of female pattern hair loss with oral antiandrogens. Br J Dermatol. 2005

Design
case series
People
80
Duration
12+ months
Who
women with female pattern hair loss

Tested: spironolactone 200 mg or cyproterone acetate (open, no placebo)

Result: 44% regrew, 44% stayed stable and 12% kept losing hair; results were similar for both drugs and no hormone level predicted response.

Read the study ↗

Ong MM et al. Antiandrogen therapy for female pattern hair loss: clinical review. 2025

Design
review
Who
women with female pattern hair loss

Tested: review of antiandrogen options

Result: Choice of antiandrogen differs by whether hormone excess (acne, hirsutism, irregular periods) is present.

Read the study ↗

Li Y et al. CG2001 (topical minoxidil-finasteride foam): phase 1. 2026

Design
rct
People
44
Who
healthy volunteers

Tested: topical minoxidil-finasteride foam

Result: Phase 1 study published in 2026.

Read the study ↗

Inventage Lab. IVL3001 (long-acting finasteride injection) pharmacokinetic study. ClinicalTrials.gov NCT04945226

Design
rct
People
40
Who
healthy volunteers

Tested: long-acting finasteride injection

Result: Registered pharmacokinetic study.

Read the study ↗

Chong Kun Dang. Phase 3 study of CKD-843 in male androgenetic alopecia. ClinicalTrials.gov NCT06916793

Design
rct
People
288
Who
Korean men with androgenetic alopecia (planned)

Tested: CKD-843 injection every 3 months vs oral dutasteride vs placebo

Result: Registered phase 3; primary completion expected September 2027.

Read the study ↗