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Comparison · NCT04535531-5258ccf5

SB206 vs Placebo: 90% Reduction From Baseline in the Number of All Treatable MC at Week 12

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. SB206 vs Placebo: 90% Reduction From Baseline in the Number of All Treatable MC at Week 12. Trial comparisons, record NCT04535531-5258ccf5. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04535531-5258ccf5

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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 10.430.3850.477wilson
Risk in group 20.2390.2020.281wilson
Risk difference, group 1 minus group 20.1910.1290.25newcombe hybrid score
Risk ratio, group 1 over group 21.81.482.19log
Odds ratio, group 1 over group 22.41.83.2log
Number needed to treat, for one more participant with the outcome on SB206 than on Placebo5.243.997.73from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1SB206SB206 gel applied topically, once daily for 12 weeks.191444OG000
Group 2PlaceboPlacebo gel applied topically, once daily for 12 weeks.107447OG001

Outcome

Type
SECONDARY
Title
90% Reduction From Baseline in the Number of All Treatable MC at Week 12
Description
Percent (proportion) of subjects achieving at least a 90% reduction from Baseline in the number of all treatable MC at Week 12
Time frame
12 Weeks
Population
ITT

Source ClinicalTrials.gov

Trial

Title
A Phase 3 Molluscum Contagiosum Efficacy and Safety Study
NCT number
NCT04535531
Phases
PHASE3
Conditions
Molluscum Contagiosum
Interventions
SB206 10.3% berdazimer, vehicle gel
Lead sponsor
Novan, Inc.
Results first posted
2023-01-26

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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