Acne vulgaris research record

What do registered trials show for acne?

10 treatments have a posted result against a comparison group. The exact treatment and comparison numbers are below.

The guide helps with care decisions. This page is the supporting trial record.

01

Treatment results

These treatments have at least one completed trial that posted a result against a comparison group — the only kind of result that can show the treatment itself made the difference. Each card is one trial against its own comparator, so cards can’t be compared head-to-head. Every result-posting study in the record was scanned, not just recent ones. A “vehicle” is the same cream or gel without the active ingredient — the fairest comparison for a topical.

Acanya Gel

21.3 more people per 100 reached the trial’s rating of treatment success at week 12.

Serious adverse events in this trial: 0 of 469 on treatment vs 1 of 237 in the comparison group (submitted counts).

Outcome: Clinical Success on Investigator's Global Evaluation · NCT01796665 details · ClinicalTrials.gov record · Phase 3 · Industry-run

Adapalene, Benzoyl Peroxide Drug Combination

20 more people per 100 reached the trial’s rating of treatment success at week 12.

Serious adverse events in this trial: 3 of 419 on treatment vs 2 of 418 in the comparison group (submitted counts).

Outcome: Success Rate on the Investigator's Global Assessment · NCT00421993 details · ClinicalTrials.gov record · Phase 3 · Industry-run

Benzoyl Peroxide

8.8 more people per 100 reached the trial’s rating of treatment success at week 12.

Serious adverse events in this trial: 3 of 419 on treatment vs 2 of 418 in the comparison group (submitted counts).

Outcome: Success Rate on the Investigator's Global Assessment · NCT00421993 details · ClinicalTrials.gov record · Phase 3 · Industry-run

Clindamycin

7.2 more people per 100 reached a better rating from the trial’s own assessor at baseline (day 1) and week 12.

Serious adverse events in this trial: 0 of 328 on treatment vs 0 of 332 in the comparison group (submitted counts).

Outcome: Number of Participants With Improvement of at Least 2 Grades in the Investigator's Static Global Assessment (ISGA) Score From Baseline to Week 12 · NCT00776919 details · ClinicalTrials.gov record · Phase 3 · Industry-run

Minocycline

6.8 more people per 100 reached clear or almost-clear skin at week 12.

Serious adverse events in this trial: 4 of 333 on treatment vs 2 of 162 in the comparison group (submitted counts).

Outcome: Percentage of Participants Achieving Investigator's Global Assessments (IGA) Treatment Success at Week 12 · NCT02815280 details · ClinicalTrials.gov record · Phase 3 · Industry-run

Adapalene

3.9 more people per 100 reached the trial’s rating of treatment success at week 12.

Serious adverse events in this trial: 1 of 418 on treatment vs 2 of 418 in the comparison group (submitted counts).

Outcome: Success Rate on the Investigator's Global Assessment · NCT00421993 details · ClinicalTrials.gov record · Phase 3 · Industry-run

4 more treatments have a comparative result — marked in the full treatment list below.

Where the comparison did as well — or better

Before paying more for a newer option, check whether it beat the alternative in its own trial. In these primary outcomes, it didn’t:

Every study with posted results in this record

21 registered acne studies posted numeric results that this index maps to a treatment. Each has its own page showing exactly what was submitted, group by group.

  • NCT00392223Minocycline
  • NCT00421993 · the trial’s rating of treatment successAdapalene, Benzoyl Peroxide, Adapalene, Benzoyl Peroxide Drug Combination
  • NCT00422240 · clear or almost-clear skinAdapalene, Benzoyl Peroxide Drug Combination
  • NCT00776919 · a better rating from the trial’s own assessorClindamycin
  • NCT00807014Adapalene, clindamycin phosphate benzoyl peroxide combination
  • NCT00829049 · fewer inflamed spotsAdapalene
  • NCT00907335 · fewer inflamed spotsTretinoin
  • NCT01138735 · fewer lesionsAdapalene, Benzoyl Peroxide Drug Combination
  • NCT01188538Adapalene, Benzoyl Peroxide Drug Combination
  • NCT01243450 · fewer lesionsTretinoin
  • NCT01796665 · the trial’s rating of treatment successAcanya Gel
  • NCT02249767 · fewer lesionsTretinoin
  • NCT02267746 · fewer lesionstazarotene
  • NCT02557399 · fewer lesionsclindamycin phosphate benzoyl peroxide combination
  • NCT02815267 · clear or almost-clear skinMinocycline
  • NCT02815280 · clear or almost-clear skinMinocycline
  • NCT02886715 · fewer inflamed spotstazarotene
  • NCT02944461 · fewer inflamed spotsDapsone
  • NCT03522441 · fewer lesionsClindamycin
  • NCT05550337 · fewer inflamed spotstrifarotene
  • NCT06415305 · clear or almost-clear skinClascoterone
Did a more expensive option beat the alternative?

Head-to-head: when treatments faced each other

Most trials compare against a placebo or vehicle. These posted outcomes compared one active treatment with another — the comparison that actually answers “which one?”:

  • DUAC -42.2% vs ADA 0.1% +CLDM 1% -35.3%Baseline (Day 1) and Week 2 · primary outcome · NCT02557399clindamycin phosphate benzoyl peroxide combination
  • Differin Gel -1.1 scores on a scale vs Duac Gel -4.9 scores on a scaleBaseline (Week 0) and Week 2 · primary outcome · NCT00807014Adapalene
  • Duac Gel -4.9 scores on a scale vs Differin Gel -1.1 scores on a scaleBaseline (Week 0) and Week 2 · primary outcome · NCT00807014clindamycin phosphate benzoyl peroxide combination
  • Adapalene Gel 0.3% -60% vs Tazarotene Cream 0.1% -68.1%Baseline, Week 12 · primary outcome · NCT00829049Adapalene

The trials nobody ran

Among the most-studied acne treatments, these pairs have never even appeared together in a registered trial — so no public evidence says which one is better:

  • AdapaleneIsotretinoin
  • Benzoyl PeroxideIsotretinoin
  • ClindamycinIsotretinoin
  • ClindamycinAdapalene, Benzoyl Peroxide Drug Combination
  • TretinoinDoxycycline
  • TretinoinAdapalene, Benzoyl Peroxide Drug Combination

Same molecule, different price tag

Regulatory status of the tracked treatments — whether the molecule studied in the trials above is available over the counter, as a generic, or brand-only. 15 of them have an OTC, generic, or biosimilar route.

TreatmentStatusUnited StatesCanada
adapalene (Differin)The OTC 0.1% gel and the prescription 0.3% gel contain the same molecule at different strengths.Available over the counterAdapalene 0.1% gel is sold OTC (Differin Gel, switched from prescription in 2016); the 0.3% gel and other strengths and forms remain prescription-only. sourcePrescription-only in Canada (Differin); no OTC adapalene product. source
adapalene + benzoyl peroxide (Epiduo, Epiduo Forte, TactuPump)The OTC gel, prescription generics, and Epiduo all pair the same two molecules at 0.1%/2.5%; Epiduo Forte uses a higher adapalene strength.Available over the counterThe 0.1%/2.5% gel was approved for OTC sale in May 2026 (Differin Epiduo, retail from summer 2026); prescription generics of the 0.1%/2.5% gel exist, and Epiduo Forte (0.3%/2.5%) remains prescription-only. sourcePrescription-only in Canada, marketed as TactuPump and TactuPump Forte. source
benzoyl peroxide (PanOxyl)OTC products and prescription combinations (with clindamycin or adapalene) use the same molecule.Available over the counterOTC at 2.5%-10% in washes, gels, and creams under the FDA topical acne monograph (M006). sourceSold without a prescription in Canada in similar strengths. source
azelaic acid (Finacea, Azelex)The 15% gel/foam (rosacea) and 20% cream (acne) contain the same molecule at different strengths; lower-strength azelaic acid also appears in cosmetics.Generic prescription availableFinacea 15% gel (rosacea) has prescription generics; the 15% foam remains brand-only; Azelex 20% cream (acne) is brand-only. sourceFinacea 15% gel is available in Canada by prescription. source
calcipotriene (calcipotriol) (Dovonex, Sorilux)Calcipotriene (US name) and calcipotriol (international name) are the same vitamin D analog.Generic prescription availableGeneric calcipotriene cream, ointment, and solution are available by prescription; also sold in combination with betamethasone (Taclonex and generics). sourceKnown as calcipotriol in Canada (Dovonex and combinations); prescription-only. source
clindamycin (Cleocin T, Clindagel, Dalacin T)Topical acne clindamycin is the same antibiotic used orally for infections, formulated for the skin.Generic prescription availableTopical gels, lotions, solutions, and foams as well as oral clindamycin are available as prescription generics. sourcePrescription-only; marketed as Dalacin T and generics. source
clindamycin phosphate (Cleocin T, Dalacin T)Clindamycin phosphate is the ester form of clindamycin used in topical products; it converts to the same active antibiotic in the skin.Generic prescription availablePrescription topical products (solution, gel, lotion, foam) are available as generics. sourcePrescription-only; marketed as Dalacin T and generics. source
clindamycin phosphate + benzoyl peroxide (BenzaClin, Duac, Onexton)Brand gels (BenzaClin, Duac, Onexton, Acanya) and their generics pair the same two molecules at varying strengths.Generic prescription availablePrescription combination gels (1%/5%, 1.2%/2.5%, 1.2%/3.75%) with generic equivalents available. sourceMarketed by prescription in Canada (e.g., Clindoxyl gel). source
clindamycin phosphate + benzoyl peroxide (Acanya)Acanya contains the same two molecules found in generic clindamycin phosphate-benzoyl peroxide gels.Generic prescription availablePrescription gel combining clindamycin phosphate 1.2% and benzoyl peroxide 2.5%; generic clindamycin-benzoyl peroxide gels are available. sourcePrescription clindamycin-benzoyl peroxide combination gels (e.g., Clindoxyl) are marketed in Canada. source
dapsone (Aczone)Topical dapsone gel and oral dapsone tablets contain the same molecule in different formulations.Generic prescription availableAczone 5% and 7.5% acne gels have prescription generic equivalents; oral dapsone tablets are also generic. sourcenot verified
doxycycline (Oracea, Vibramycin, Apprilon)The 40 mg modified-release rosacea capsule contains the same molecule as generic immediate-release doxycycline, at a sub-antimicrobial dose.Generic prescription availableOral doxycycline (used at antibiotic doses for acne) is a widely available generic; the 40 mg modified-release anti-inflammatory capsule for rosacea (Oracea) has had generics since 2024. sourceGeneric oral doxycycline is available by prescription; the 40 mg modified-release form is marketed as Apprilon. source
isotretinoin (Absorica, Accutane, Epuris)All isotretinoin capsule brands and generics contain the same molecule; low-dose use in rosacea is off-label in both markets.Generic prescription availableOral isotretinoin is generic (e.g., Claravis, Amnesteem, Absorica) and dispensed under the iPLEDGE safety program; rosacea use is off-label. sourceAvailable by prescription as brands (Accutane, Clarus, Epuris) and generics. source
metformin (Glucophage)No metformin product is approved for melasma in the US or Canada; trial use involves the same molecule sold generically for diabetes.Generic prescription availableGeneric prescription tablets approved for type 2 diabetes; use for melasma (topical or oral) is off-label/investigational. sourceGeneric prescription metformin is available in Canada for diabetes; melasma use is off-label. source
minocycline (Minocin, Solodyn, Amzeeq)The brand-only 4% topical foam and generic oral capsules contain the same antibiotic.Generic prescription availableOral minocycline, including extended-release tablets, is generic by prescription; the 4% topical foam (Amzeeq, approved 2019) is brand-only. sourceOral minocycline is generic by prescription in Canada. source
tretinoin (Retin-A, Altreno, Stieva-A)Prescription generics and brands contain the same molecule; unlike adapalene, no tretinoin product is sold OTC in the US or Canada.Generic prescription availableTopical tretinoin creams and gels (0.01%-0.1%) are prescription generics; for melasma, tretinoin alone is off-label but it is one of the three molecules in the approved combination Tri-Luma. sourcePrescription-only; available as brands (Retin-A, Stieva-A) and generics. source
apremilast (Otezla)Apremilast is a small-molecule tablet but currently has no marketed US generic.Brand-only prescriptionOtezla tablets are brand-only by prescription; no generic is currently marketed in the US. sourceOtezla is available by prescription in Canada. source
clascoterone (Winlevi)Clascoterone is available only as the brand Winlevi in both markets.Brand-only prescriptionWinlevi 1% cream (approved 2020) is prescription-only; no generic is available. sourceWinlevi 1% cream approved by Health Canada in June 2023; prescription-only. source
sarecycline (Seysara)Sarecycline is a narrow-spectrum tetracycline sold only as the brand Seysara, unlike doxycycline and minocycline, which are generic.Brand-only prescriptionSeysara tablets are brand-only by prescription; no generic. sourcenot verified

Regulatory status only, verified 2026-08-20 with one source per claim — not pricing, coverage, or a recommendation. Status can change; check the linked source.

Find one of 129 tracked treatments

Search by brand or generic name, or browse the 60 most-studied terms. They are ordered by what the public record can show, not by benefit or safety.

AdapaleneAvailable over the counter3 comparative results · 28 result-posting studies scanned54 linked records · 26 of 44 completed posted results

At week 12, 21.8% of people in the Adapalene Gel group had the submitted improvement result (Success Rate on the Investigator's Global Assessment), compared with 17.9% in the Gel Vehicle group—3.9 more people per 100.

One submitted registry outcome, not a pooled estimate — from NCT00421993 details · ClinicalTrials.gov record · Phase 3 · Industry lead sponsor · vs placebo/vehicle · earliest favourable time point: week 12

Who was in these trials?
  • Average age 19.7 years (submitted means covering 5,384 participants).
  • 59% of 7,143 counted participants were female.
  • Race or ethnicity reported in 8 studies; skin phototype in 1.
  • Fitzpatrick IV–VI (darker skin) reported: yes — 50 participants across the reporting studies.
Benzoyl PeroxideAvailable over the counter1 comparative result · 28 result-posting studies scanned43 linked records · 25 of 36 completed posted results

At week 12, 26.7% of people in the Benzoyl Peroxide Gel group had the submitted improvement result (Success Rate on the Investigator's Global Assessment), compared with 17.9% in the Gel Vehicle group—8.8 more people per 100.

One submitted registry outcome, not a pooled estimate — from NCT00421993 details · ClinicalTrials.gov record · Phase 3 · Industry lead sponsor · vs placebo/vehicle · earliest favourable time point: week 12

Who was in these trials?
  • Average age 20 years (submitted means covering 6,413 participants).
  • 59% of 7,764 counted participants were female.
  • Race or ethnicity reported in 5 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
ClindamycinGeneric prescription available6 comparative results · 17 result-posting studies scanned34 linked records · 17 of 32 completed posted results

At Baseline (Day 1) and Week 12, 25% of people in the Clindamycin Gel group had the submitted improvement result (Number of Participants With Improvement of at Least 2 Grades in the Investigator's Static Global Assessment (ISGA) Score From Baseline to Week 12), compared with 17.8% in the Vehicle Gel group—7.2 more people per 100.

One submitted registry outcome, not a pooled estimate — from NCT00776919 details · ClinicalTrials.gov record · Phase 3 · Industry lead sponsor · vs placebo/vehicle · earliest favourable time point: week 12

Who was in these trials?
  • Average age 20.7 years (submitted means covering 8,869 participants).
  • 58% of 9,296 counted participants were female.
  • Race or ethnicity reported in 5 studies; skin phototype in 1.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
Adapalene, Benzoyl Peroxide Drug CombinationAvailable over the counter5 comparative results · 14 result-posting studies scanned18 linked records · 13 of 18 completed posted results

At week 12, 37.9% of people in the Adapalene/Benzoyl Peroxide Gel group had the submitted improvement result (Success Rate on the Investigator's Global Assessment), compared with 17.9% in the Gel Vehicle group—20 more people per 100.

One submitted registry outcome, not a pooled estimate — from NCT00421993 details · ClinicalTrials.gov record · Phase 3 · Industry lead sponsor · vs placebo/vehicle · earliest favourable time point: week 12

Who was in these trials?
  • Average age 18.2 years (submitted means covering 4,626 participants).
  • 53% of 4,699 counted participants were female.
  • Race or ethnicity reported in 4 studies; skin phototype in 1.
  • Fitzpatrick IV–VI (darker skin) reported: yes — 50 participants across the reporting studies.
TretinoinGeneric prescription available5 comparative results · 12 result-posting studies scanned26 linked records · 11 of 20 completed posted results

At 12 week, Acne Lesion Percent Reduction changed by -53.5% in the Brand group and -35% in the Placebo group—a difference 18.5 percentage points numerically larger in the selected group.

One submitted registry outcome, not a pooled estimate — from NCT01243450 details · ClinicalTrials.gov record · Phase 3 · Industry lead sponsor · vs placebo/vehicle · earliest favourable time point: week 12

Who was in these trials?
  • Average age 20.5 years (submitted means covering 2,704 participants).
  • 59% of 4,155 counted participants were female.
  • Race or ethnicity reported in 1 study; skin phototype in 2.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
clindamycin phosphate benzoyl peroxide combinationGeneric prescription available2 comparative results · 10 result-posting studies scanned13 linked records · 10 of 13 completed posted results

At Baseline (Day 1) and Week 2, Percent Change in Total Lesion Counts (TLs) From Baseline to Week 2 changed by -42.2% in the DUAC group and -35.3% in the ADA 0.1% +CLDM 1% group—a difference 6.9 percentage points numerically larger in the selected group.

One submitted registry outcome, not a pooled estimate — from NCT02557399 details · ClinicalTrials.gov record · Phase 4 · Industry lead sponsor · vs another active treatment

Who was in these trials?
  • Average age 20.4 years (submitted means covering 4,082 participants).
  • 58% of 4,250 counted participants were female.
  • Race or ethnicity reported in 5 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
tazarotene6 comparative results · 8 result-posting studies scanned13 linked records · 8 of 12 completed posted results

At Week 12, Change in Inflammatory Lesion Counts changed by -58.4% in the Test group and -53.3% in the Placebo group—a difference 5.1 percentage points numerically larger in the selected group.

One submitted registry outcome, not a pooled estimate — from NCT02886715 details · ClinicalTrials.gov record · Phase 3 · Industry lead sponsor · vs placebo/vehicle · earliest favourable time point: week 12

Who was in these trials?
  • Average age 21.4 years (submitted means covering 3,635 participants).
  • 45% of 3,806 counted participants were female.
  • Race or ethnicity reported in 4 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
MinocyclineGeneric prescription available4 comparative results · 7 result-posting studies scanned14 linked records · 6 of 11 completed posted results

At Baseline and Week 12, 14.7% of people in the FMX-101, 4% Minocycline Foam group had the submitted improvement result (Percentage of Participants Achieving Investigator's Global Assessments (IGA) Treatment Success at Week 12), compared with 7.9% in the Vehicle Foam group—6.8 more people per 100.

One submitted registry outcome, not a pooled estimate — from NCT02815280 details · ClinicalTrials.gov record · Phase 3 · Industry lead sponsor · vs placebo/vehicle · earliest favourable time point: week 8

Who was in these trials?
  • Average age 20.5 years (submitted means covering 1,003 participants).
  • 60% of 2,491 counted participants were female.
  • Race or ethnicity reported in 5 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
trifarotene3 comparative results · 7 result-posting studies scanned9 linked records · 6 of 8 completed posted results

At Baseline and 12 Weeks, Primary Change in Inflammatory Lesion Counts changed by -72.9% in the Test: Trifarotene Cream, 0.005% group and -34.1% in the Vehicle Product group—a difference 38.8 percentage points numerically larger in the selected group.

One submitted registry outcome, not a pooled estimate — from NCT05550337 details · ClinicalTrials.gov record · Phase 3 · Industry lead sponsor · vs placebo/vehicle · earliest favourable time point: week 12

Who was in these trials?
  • Average age 18.7 years (submitted means covering 553 participants).
  • 51% of 3,426 counted participants were female.
  • Race or ethnicity reported in 6 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
Acanya GelGeneric prescription available1 comparative result · 2 result-posting studies scanned3 linked records · 2 of 2 completed posted results

At Baseline to week 12, 35.4% of people in the Reference Product group had the submitted improvement result (Clinical Success on Investigator's Global Evaluation), compared with 14.1% in the Placebo Product group—21.3 more people per 100.

One submitted registry outcome, not a pooled estimate — from NCT01796665 details · ClinicalTrials.gov record · Phase 3 · Industry lead sponsor · vs placebo/vehicle · earliest favourable time point: week 12

Who was in these trials?
  • Average age 19.8 years (submitted means covering 1,180 participants).
  • 56% of 1,216 counted participants were female.
  • Race or ethnicity reported in 1 study; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
ClascoteroneBrand-only prescriptionWithin-group result only14 linked records · 11 of 11 completed posted results
Who was in these trials?
  • Average age 19.5 years (submitted means covering 2,514 participants).
  • 62% of 2,604 counted participants were female.
  • Race or ethnicity reported in 8 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
DapsoneGeneric prescription availableWithin-group result only17 linked records · 10 of 15 completed posted results
Who was in these trials?
  • Average age 16.5 years (submitted means covering 172 participants).
  • 73% of 937 counted participants were female.
  • Race or ethnicity reported in 2 studies; skin phototype in 1.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
DoxycyclineGeneric prescription availablePosted results · no safely mapped effect in any scanned study22 linked records · 11 of 16 completed posted results
Who was in these trials?
  • Average age 19.4 years (submitted means covering 1,849 participants).
  • 47% of 2,221 counted participants were female.
  • Race or ethnicity reported in 5 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
clindamycin phosphateGeneric prescription availablePosted results · no safely mapped effect in any scanned study14 linked records · 5 of 10 completed posted results
Who was in these trials?
  • Average age 19.9 years (submitted means covering 1,246 participants).
  • 51% of 2,132 counted participants were female.
  • Race or ethnicity reported in 1 study; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
IsotretinoinGeneric prescription availablePosted results · no safely mapped effect in any scanned study19 linked records · 4 of 12 completed posted results
Who was in these trials?
  • Average age 20.3 years (submitted means covering 1,414 participants).
  • 35% of 1,414 counted participants were female.
  • Race or ethnicity reported in 1 study; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
berdazimer sodiumPosted results · no safely mapped effect in any scanned study13 linked records · 4 of 13 completed posted results
Who was in these trials?
  • Average age 21.3 years (submitted means covering 3,390 participants).
  • 60% of 3,446 counted participants were female.
  • Race or ethnicity reported in 4 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
Salicylic AcidPosted results · no safely mapped effect in any scanned study11 linked records · 4 of 9 completed posted results
Who was in these trials?
  • Average age 21.9 years (submitted means covering 68 participants).
  • 81% of 185 counted participants were female.
  • Race or ethnicity reported in 2 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
1-phenyl-3,3-dimethyltriazenePosted results · no safely mapped effect in any scanned study7 linked records · 4 of 7 completed posted results
Who was in these trials?
  • Average age 18.6 years (submitted means covering 153 participants).
  • 52% of 430 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 4.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
sarecyclineBrand-only prescriptionPosted results · no safely mapped effect in any scanned study5 linked records · 4 of 4 completed posted results
Who was in these trials?
  • Average age 20.2 years (submitted means covering 285 participants).
  • 56% of 2,770 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
drospirenone and ethinyl estradiol combinationPosted results · no safely mapped effect in any scanned study4 linked records · 2 of 4 completed posted results
Who was in these trials?
  • Average age 23.7 years (submitted means covering 173 participants).
  • 100% of 203 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
clindamycin, tretinoin drug combinationPosted results · no safely mapped effect in any scanned study3 linked records · 2 of 3 completed posted results
Who was in these trials?
  • Average age 23.1 years (submitted means covering 26 participants).
  • 61% of 87 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
Red LightPosted results · no safely mapped effect in any scanned study3 linked records · 2 of 2 completed posted results
Who was in these trials?
  • Average age 18.6 years (submitted means covering 153 participants).
  • 48% of 260 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 2.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
Ethinyl EstradiolPosted results · no safely mapped effect in any scanned study2 linked records · 2 of 2 completed posted results
Who was in these trials?
  • 100% of 231 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
methyl 5-aminolevulinatePosted results · no safely mapped effect in any scanned study2 linked records · 2 of 2 completed posted results
Who was in these trials?
  • 59% of 170 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 2.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
Aminolevulinic AcidPosted results · no safely mapped effect in any scanned study4 linked records · 1 of 4 completed posted results
Who was in these trials?
  • 52% of 266 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 1.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
azelaic acidGeneric prescription availablePosted results · no safely mapped effect in any scanned study3 linked records · 1 of 3 completed posted results
Who was in these trials?
  • Average age 20.1 years (submitted means covering 217 participants).
  • 55% of 217 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
drospirenonePosted results · no safely mapped effect in any scanned study3 linked records · 1 of 3 completed posted results
Who was in these trials?
  • 100% of 30 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
ExercisePosted results · no safely mapped effect in any scanned study3 linked records · 1 of 3 completed posted results
Who was in these trials?
  • Average age 22.2 years (submitted means covering 294 participants).
  • 63% of 287 counted participants were female.
  • Race or ethnicity reported in 1 study; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
CarnitinePosted results · no safely mapped effect in any scanned study2 linked records · 1 of 2 completed posted results
Who was in these trials?
  • Average age 27.5 years (submitted means covering 120 participants).
  • 56% of 120 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
PhototherapyPosted results · no safely mapped effect in any scanned study2 linked records · 1 of 1 completed posted results
Who was in these trials?
  • Average age 26.5 years (submitted means covering 60 participants).
  • 0% of 60 counted participants were female.
  • Race or ethnicity reported in 1 study; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
1,7-bis(4-hydroxy-3-methoxyphenyl)-1,4,6-heptatrien-3-onePosted results · no safely mapped effect in any scanned study1 linked record · 1 of 1 completed posted results
Who was in these trials?
  • Average age 21.3 years (submitted means covering 181 participants).
  • 48% of 181 counted participants were female.
  • Race or ethnicity reported in 1 study; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
Acne RA-1,2Posted results · no safely mapped effect in any scanned study1 linked record · 1 of 1 completed posted results
Who was in these trials?
  • Average age 22.9 years (submitted means covering 33 participants).
  • 48% of 33 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
afamelanotidePosted results · no safely mapped effect in any scanned study1 linked record · 1 of 1 completed posted results
Who was in these trials?
  • 0% of 3 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
calcipotrieneGeneric prescription availablePosted results · no safely mapped effect in any scanned study1 linked record · 1 of 1 completed posted results
Who was in these trials?
  • 68% of 65 counted participants were female.
  • Race or ethnicity reported in 1 study; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
DesogestrelPosted results · no safely mapped effect in any scanned study1 linked record · 1 of 1 completed posted results
Who was in these trials?
  • 100% of 201 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
EthanolPosted results · no safely mapped effect in any scanned study1 linked record · 1 of 1 completed posted results
Who was in these trials?
  • Average age 20.1 years (submitted means covering 12 participants).
  • 50% of 12 counted participants were female.
  • Race or ethnicity reported in 1 study; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
eucerinPosted results · no safely mapped effect in any scanned study1 linked record · 1 of 1 completed posted results
Who was in these trials?
  • Average age 27.5 years (submitted means covering 120 participants).
  • 56% of 120 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
gluconic acidPosted results · no safely mapped effect in any scanned study1 linked record · 1 of 1 completed posted results
Who was in these trials?
  • 75% of 16 counted participants were female.
  • Race or ethnicity reported in 1 study; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
licochalcone APosted results · no safely mapped effect in any scanned study1 linked record · 1 of 1 completed posted results
Who was in these trials?
  • Average age 27.5 years (submitted means covering 120 participants).
  • 56% of 120 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
LymecyclinePosted results · no safely mapped effect in any scanned study1 linked record · 1 of 1 completed posted results
Who was in these trials?
  • Average age 18.9 years (submitted means covering 378 participants).
  • 45% of 378 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
norgestimatePosted results · no safely mapped effect in any scanned study1 linked record · 1 of 1 completed posted results
Who was in these trials?
  • 100% of 201 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
Pharmaceutical PreparationsPosted results · no safely mapped effect in any scanned study1 linked record · 1 of 1 completed posted results
Who was in these trials?
  • Average age 19.8 years (submitted means covering 1,180 participants).
  • 56% of 1,180 counted participants were female.
  • Race or ethnicity reported in 1 study; skin phototype in 0.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
TriclosanPosted results · no safely mapped effect in any scanned study1 linked record · 1 of 1 completed posted results
Who was in these trials?
  • 51% of 247 counted participants were female.
  • Race or ethnicity reported in 0 studies; skin phototype in 1.
  • Fitzpatrick IV–VI (darker skin) reported: not in any tracked study — the record does not say how well this was tested on darker skin.
17 more tracked treatments with no posted results — studied, but the public record holds no numbers yet
AzithromycinNo posted results5 linked records · 0 of 2 completed posted results
PhotochemotherapyNo posted results5 linked records · 0 of 4 completed posted results
SpironolactoneNo posted results3 linked records · 0 of 1 completed posted results
apremilastBrand-only prescriptionNo posted results2 linked records · 0 of 1 completed posted results
Lasers, ExcimerNo posted results2 linked records · 0 of 1 completed posted results
lupeolNo posted results2 linked records · 0 of 2 completed posted results
MetforminGeneric prescription availableNo posted results2 linked records · 0 of 1 completed posted results
retinol palmitateNo posted results2 linked records · 0 of 1 completed posted results
TriamcinoloneNo posted results2 linked records · 0 of 1 completed posted results
acebilustatNo posted results1 linked record · 0 of 1 completed posted results
bermekimabNo posted results1 linked record · 0 of 1 completed posted results
capryloyl salicylic acidNo posted results1 linked record · 0 of 1 completed posted results
CyproteroneNo posted results1 linked record · 0 of 1 completed posted results
Cyproterone acetate, ethinyl estradiol drug combinationNo posted results1 linked record · 0 of 1 completed posted results
Diet, Fat-RestrictedNo posted results1 linked record · 0 of 1 completed posted results
Diet, VeganNo posted results1 linked record · 0 of 1 completed posted results
Drugs, GenericNo posted results1 linked record · 0 of 1 completed posted results

02

Who was studied?

Only 21 of 200 result-posting acne studies reported participants’ separately measured skin type. The public record therefore rarely shows whether people with skin like yours were included.

Among 200 completed studies with posted results, this is how often each participant detail was reported.

Age reported — 200 of 200 studies100%
Age reported — 200 of 200 studies
Sex or gender reported — 200 of 200 studies100%
Sex or gender reported — 200 of 200 studies
Race or ethnicity reported — 127 of 200 studies64%
Race or ethnicity reported — 127 of 200 studies
Skin phototype reported — 21 of 200 studies11%
Skin phototype reported — 21 of 200 studies
Who could enrol — eligible age bands (studies)
  • Adults eligible618
  • Children eligible392
  • Older adults eligible253
Who could enrol — sex eligibility (studies)
  • All sexes eligible581
  • Female participants eligible35
  • Male participants eligible15

03

Research record

Open the part you need. Every count remains tied to this condition and snapshot.

200 of 465 completed trials posted results
200 of 465 completed studies posted results43%
200 of 465 completed studies posted results

265 completed trials did not post numeric results to the registry as of 2026-09-11. A missing result does not mean the treatment failed; it means the public cannot check what happened.

Among studies that ended at least 12 months ago, 200 of 442 (45.2%) posted results.

Who ran the trials and how they were designed

65% were led by industry, usually the company selling the treatment. This is context about who asked the question, not proof that a result is wrong.

Registered trial phases (studies)
  • Not applicable173
  • Phase 3125
  • Phase 4114
  • Phase 2101
  • Phase 175
  • Phase 1 / Phase 223
  • Early phase 113
  • Phase 2 / Phase 37
Lead sponsor class (studies)
  • Industry411
  • Other organization200
  • Other government9
  • Research network6
  • Individual5

Lead sponsor class is not the same as all funding, and it is not a study-quality score.

Timelines and 57 active or recruiting trials

Across 322 primary-outcome time points, the typical trial judged success around week 12. This record does not support a claim of visible results in days.

Registered study starts per year

Acne vulgaris registered study starts per year, 2000–2027
2000–2027 · 2027: 1

Median study duration: 10 months.

Study starts by year (table)
YearStudy starts
20001
20011
20022
20034
20048
200511
200615
200715
200829
200940
201032
201130
201225
201328
201431
201539
201641
201723
201827
201923
202029
202128
202224
202333
202439
202528
202622
20271
Most-listed study countries (of 56 total)
  • United States322
  • Canada52
  • China31
  • Egypt24
  • Germany16
  • Brazil15
  • Poland15
  • France14
  • +4 more43

Study locations are not participant nationality or ancestry.

Study counts, sources and limits
clinical trials tracked
631
completed trials with posted results
200 of 465
submitted enrollment
136,403
active or recruiting now
57

ClinicalTrials.gov data through · methodology v2.1.0 · snapshot 9a17314144e5…

What these figures cannot tell you

  • Registry records are submitted by sponsors and investigators; Skinlogie processes selected fields but does not independently verify every record.
  • Nothing here is a pooled estimate of whether one treatment works better or causes fewer harms — results stay tied to their single study, outcome, comparator, and time point.
  • “Completed” is a registry status, not a judgment of study quality, risk of bias, or selective reporting; posted results are not the complete journal literature.
  • Study counts and research activity measure how much research is visible, not how well a treatment works.
  • Enrollment sums count submitted participant entries, not guaranteed unique people; reported categories cannot show whether a population was representative or whether subgroup findings apply to you.
  • A between-group difference can estimate a comparative effect only when groups and outcome are clear enough; a percentage observed in a single group cannot show what would have happened without treatment.
  • This index cannot decide whether a treatment is safe or suitable for you — that depends on benefits and harms, your preferences, and your health context.

Plain-language definitions

Placebo
A look-alike with no medicine in it, so trials can separate the treatment’s effect from expectation and time.
Vehicle
The same cream or gel without the active ingredient — the fair comparison for topicals, because the base alone can moisturize.
Comparative result
A posted number for the treatment group and a comparison group in the same trial. Only this kind of result can show the treatment itself made the difference.
Primary outcome
The one measurement a trial named in advance as its test of success — harder to cherry-pick than outcomes chosen after the fact.
Phase 3
The large, late-stage trials regulators rely on. Phase 1 and 2 are smaller and earlier; Phase 4 studies happen after approval.
Industry-run
The registered lead sponsor is a company — usually the one selling the treatment. Not proof of bias, but worth knowing who asked the question.
Biosimilar
A close copy of a biologic drug approved as equivalent — the “generic” route for biologics, typically sold at a lower price.
n=
How many people were analysed in a group. Bigger groups give steadier numbers.

Source: official ClinicalTrials.gov search · snapshot · result-mapping layer (v1.1.0, 2026-08-21) · field guide and citation.

Cite or reuse this resultCopy the dated, source-linked sentence

Citation text

As of 2026-09-11, 200 of 465 completed acne trials registered on ClinicalTrials.gov have posted results, and 10 treatments have a posted result against a comparison group (Skinlogie Evidence Index, https://skinlogie.com/evidence-index/acne).

Skinlogie’s derived figures are licensed CC BY 4.0 — reuse them with this attribution. Source records: ClinicalTrials.gov. Full dataset and citation format →