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Comparison · NCT03377790-d9ed9af2

VP-102 vs Placebo: Subject Reported Spread to Household Members as Measured by Any New Occurrence of Molluscum in Household Members of Subject.

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. VP-102 vs Placebo: Subject Reported Spread to Household Members as Measured by Any New Occurrence of Molluscum in Household Members of Subject. Trial comparisons, record NCT03377790-d9ed9af2. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03377790-d9ed9af2

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.05630.02990.103wilson
Risk in group 20.1230.07310.199wilson
Risk difference, group 1 minus group 2-0.0664-0.1470.00203newcombe hybrid score
Risk ratio, group 1 over group 20.4590.2031.03log
Odds ratio, group 1 over group 20.4260.1751.04log
Number needed to treat, for one fewer participant with the outcome on VP-102 than on Placebo15.1from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1VP-102
VP-102 Film Forming Solution applied via a prefilled applicator to affected area every 21 days~VP-102: VP-102, a single-use drug device combination product containing (cantharidin) topical solution, 0.7% (w/v). VP-102 Active will be administered to Molluscum lesions
9160OG000
Group 2Placebo
Vehicle Film Forming Solution applied via a prefilled applicator to affected area every 21 days~Placebo: Placebo a single-use drug device combination product containing only the vehicle will be administered to Molluscum lesions
13106OG001

Outcome

Type
OTHER_PRE_SPECIFIED
Title
Subject Reported Spread to Household Members as Measured by Any New Occurrence of Molluscum in Household Members of Subject.
Description
Subject reported spread to household members as measured by any new occurrence of molluscum in household members of subject. To be eligible for assessment, subjects had to have at least one household member free of lesions at baseline and have at least 1 post baseline assessment of spread of molluscum lesions.
Time frame
Days 1, 21, 42, 63 and 84 (EOS).
Population
ITT Population

Source ClinicalTrials.gov

Trial

Title
Cantharidin Application in Molluscum Patients-1
NCT number
NCT03377790
Phases
PHASE3
Conditions
Molluscum Contagiosum
Interventions
VP-102 - Cantharidin, Topical Film Forming Solution, Placebo -Topical Film Forming Solution without VP-102
Lead sponsor
Verrica Pharmaceuticals Inc.
Results first posted
2021-12-14

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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