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Trial · NCT06336603

Results by group40

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
The Primary Endpoint of This Study is the Percent of Patients Who Achieve Clear or Almost Clear on IGA at Week 16.Winlevi (Clascoterone) 1% & Adapalene 0.3% Gel65percentage of participants
Percent of Total Lesion Reduction at Week 16 Compared to BaselineWinlevi (Clascoterone) 1% & Adapalene 0.3% Gel87.3Standard Deviation 11.4Percentage change
Percent of Inflammatory Lesion Reduction at Week 16 Compared to BaselineWinlevi (Clascoterone) 1% & Adapalene 0.3% Gel90.5Standard Deviation 10.1percentage change
Percent of Non-inflammatory Lesion Reduction at Week 16 Compared to BaselineWinlevi (Clascoterone) 1% & Adapalene 0.3% Gel84.8Standard Deviation 13.5percentage change
Tolerability Measures of Erythema Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelBaseline76percentage of participants
Tolerability Measures of Erythema Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelWeek 488percentage of participants
Tolerability Measures of Erythema Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelWeek 8100percentage of participants
Tolerability Measures of Erythema Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelWeek 12100percentage of participants
Tolerability Measures of Erythema Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelWeek 1694percentage of participants
Tolerability Measures of Erythema Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelWeek 20100percentage of participants
Tolerability Measures of Dryness Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelBaseline100percentage of participants
Tolerability Measures of Dryness Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelWeek 4100percentage of participants
Tolerability Measures of Dryness Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelWeek 8100percentage of participants
Tolerability Measures of Dryness Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelWeek 12100percentage of participants
Tolerability Measures of Dryness Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelWeek 16100percentage of participants
Tolerability Measures of Dryness Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelWeek 20100percentage of participants
Tolerability Measures of Peeling Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelBaseline100percentage of participants
Tolerability Measures of Peeling Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelWeek 4100percentage of participants
Tolerability Measures of Peeling Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelWeek 8100percentage of participants
Tolerability Measures of Peeling Based on 5-point Severity ScaleWinlevi (Clascoterone) 1% & Adapalene 0.3% GelWeek 12100percentage of participants

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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