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Trial · NCT01268527

Results by group160

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

OutcomeGroupCategoryValueSpreadUnits
Change in Thickness of the Psoriatic Infiltrate From Baseline to Day 80.03% E6201 Gel-92.995% Confidence Interval -200.1 to 14.3um
Change in Thickness of the Psoriatic Infiltrate From Baseline to Day 80.05% E6201 Gel-190.395% Confidence Interval -243.6 to -136.9um
Change in Thickness of the Psoriatic Infiltrate From Baseline to Day 80.1% E6201 Gel-108.095% Confidence Interval -162.9 to -53.1um
Change in Thickness of the Psoriatic Infiltrate From Baseline to Day 80.2% E6201 Gel-102.795% Confidence Interval -172.6 to -32.9um
Clinical (Global) Assessment of Efficacy at Day 12/DiscontinuationDaivonex (Calcipotriene Cream)Worsened0Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/DiscontinuationE6201 VehicleWorsened0Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/Discontinuation0.005% E6201 GelWorsened0Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/Discontinuation0.01% E6201 GelWorsened0Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/Discontinuation0.03% E6201 GelWorsened0Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/Discontinuation0.05% E6201 GelWorsened0Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/Discontinuation0.1% E6201 GelWorsened0Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/Discontinuation0.2% E6201 GelWorsened0Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/DiscontinuationDaivonex (Calcipotriene Cream)Unchanged (no effect)6.7Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/DiscontinuationE6201 VehicleUnchanged (no effect)90.0Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/Discontinuation0.005% E6201 GelUnchanged (no effect)20.0Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/Discontinuation0.01% E6201 GelUnchanged (no effect)0Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/Discontinuation0.03% E6201 GelUnchanged (no effect)6.7Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/Discontinuation0.05% E6201 GelUnchanged (no effect)0Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/Discontinuation0.1% E6201 GelUnchanged (no effect)0Percentage of participants
Clinical (Global) Assessment of Efficacy at Day 12/Discontinuation0.2% E6201 GelUnchanged (no effect)0Percentage of participants

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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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