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Trial · NCT03487549

Outcomes21

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYCohort 1: Proportion of Subjects Exhibiting Complete Clearance of All Treatable Warts (Baseline and New) at the EOS Visit (Day 84)Treatment Visit Day 1 (Baseline) compared to Day 84 (EOS) Visit.ITT PopulationParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYCohort 2: Proportion of Subjects Exhibiting Complete Clearance of All Treatable Warts (Baseline and New) at the EOT Visit (Day 84)Compare Treatment Visit 1 (Baseline) to EOT Visit (Day 84)ITT PopulationParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCohort 1: Change From Baseline in the Number of Treatable Warts (Baseline and New) at the EOS Visit (Day 84)Change in the number of warts compared at Baseline (Visit 1) to the End of Study Visit (Day 84).ITT PopulationNumber of wartsMEAN
SECONDARYCohort 1: Percent Change From Baseline in the Number of Treatable Warts (Baseline and New) at the EOT Visit (Day 84).Baseline (Visit 1) to End of Treatment Visit (Day 84).ITT PopulationPercent changeMEAN
SECONDARYCohort 1: Proportion of Subjects Exhibiting Complete Clearance of All Treatable Warts (Baseline and New) at Visit 2, Visit 3, Visit 4 and Over the Duration of the StudyBaseline, Day 14, 28, 42 and 84 (EOS)ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCohort 2: Change From Baseline in the Number of Treatable Warts (Baseline and New) at the EOT Visit Day 84)Baseline, Day 84 (EOS)ITT Populationchange in wart countMEAN
SECONDARYCohort 2: Change From Baseline in the Percent of Treatable Warts (Baseline and New) at the EOT Visit (Day 84)Baseline (Visit 1) to End of Treatment Visit (Day 84).ITT Populationpercentage of change in wart countMEAN
SECONDARYCohort 2: Proportion of Subjects Exhibiting Complete Clearance of All Treatable Warts, (Baseline and New), at Visit 2, Visit 3, Visit 4 and Over the Duration of the StudyBaseline, Day 21, 42, 63, and 84 (EOS), 105, 126, and 147ITT PopulationParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDCohort 1:Percent Reduction of All Treatable Warts (Baseline and New) From Baseline at Visit 2, Visit 3, Visit 4 and Over the Duration of the Study.Baseline, Day 14, 28, 42, and 84 (EOS)ITT PopulationPercent change in number of wartsMEAN
OTHER_PRE_SPECIFIEDCohort 1: Change From Baseline in the Number of Treatable Warts (Baseline and New) at Visit 2, Visit 3, Visit 4 and the EOS VisitBaseline, Day 14, 28, 42, and 84 (EOS)ITT Populationchange in wart countMEAN
OTHER_PRE_SPECIFIEDCohort 1: Proportion of Subjects Exhibiting ≥ 50% Clearance of All Treatable Warts (Baseline and New) at the EOS Visit as Compared to BaselineCompare Treatment Visit 1 (Baseline) to End of Study (Day 84).ITT PopulationParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDCohort 1-Proportion of Subjects Who Respond to Treatment Defined by a ≥ 50% Reduction in Total Wart Area at EOS Compared to BaselineBaseline, Day 14, 28, 42, and 84 (EOS)ITT PopulationParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDCohort 1-Proportion of Subjects Exhibiting Reduction of at Least 1 Treatable Wart From Baseline at Visit 2, Visit 3, Visit 4 and at the EOS Visit (Day 84)Baseline, Day 14, 28, 42, and 84 (EOS)ITT PopulationParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDCohort 2: Percent Reduction of All Treatable Warts (Baseline and New) From Baseline at Visit 2, Visit 3, Visit 4 and Over Duration of the Study.Baseline to Treatment Visits 2 (Day 21), 3 (Day 42), 4 (Day 63) through the End of Treatment (Day 84).ITT populationpercentage of change in wart countMEAN
OTHER_PRE_SPECIFIEDCohort 2: Change From Baseline in the Number of Treatable Warts (Baseline and New) at Treatment Visit 2, Treatment Visit 3, Treatment Visit 4 and the EOT Visit (Day 84)Baseline, Day 14, 28, 42, and 84 (EOS)ITT Populationchange in wart countMEAN
OTHER_PRE_SPECIFIEDCohort 2: Proportion of Subjects Exhibiting ≥ 50 % Clearance of All Treatable Warts (Baseline and New) at the EOT Visit (Day 84) as Compared to BaselineBaseline to Day 84 (EOT)ITT PopulationParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDCohort 2: Proportion of Subjects Who Respond to Treatment Defined by a ≥ 50% Reduction in Total Wart Area at EOT Compared to BaselineBaseline to EOT (Day 84)ITT PopulationParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDCohort 2: Proportion of Subjects Exhibiting Reduction of at Least 1 Treatable Wart From Baseline at Visit 2, Visit 3, Visit 4 and at the EOT Visit (Day 84)Baseline, Day 14, 28, 42, and 84 (EOS)ITT PopulationParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDCohort 2: Proportion of Subjects Exhibiting Complete Clearance of All Treatable Warts (Baseline and New) at Follow-up Visits on Day 105, Day 126 and Day 147Treatment Visit 1 (Baseline) to each follow-up visit Day 105, Day 126 and Day 147.ParticipantsCOUNT_OF_PARTICIPANTS
OTHER_PRE_SPECIFIEDCohort 2: Percent Reduction of All Treatable Warts (Baseline and New) From Baseline at Follow-up Visits on Day 105, Day 126 and Day 147Baseline to follow-up visits on Day 105, Day 126 and Day 147ITT Populationpercentage change from BaselineMEAN

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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