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Comparison · NCT01926496-ede911f7

Ingenol Mebutate vs Imiquimod: Number of Participants With Partial Clearance of AK Lesions

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. Ingenol Mebutate vs Imiquimod: Number of Participants With Partial Clearance of AK Lesions. Trial comparisons, record NCT01926496-ede911f7. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01926496-ede911f7

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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 10.8130.7580.857wilson
Risk in group 20.8570.8080.895wilson
Risk difference, group 1 minus group 2-0.0446-0.1110.0217newcombe hybrid score
Risk ratio, group 1 over group 20.9480.8761.03log
Odds ratio, group 1 over group 20.7220.4461.17log
Number needed to treat, for one fewer participant with the outcome on Ingenol Mebutate than on Imiquimod22.4from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Ingenol Mebutate
Arm A: Ingenol mebutate gel 0.015% applied daily for 3 consecutive days to the selected treatment area followed by 8 weeks' rest. Retreatment for another 3 consecutive days if the treatment field is not completely cleared of AKs at Week 8 \>~\> Ingenol Mebutate Gel, 0.015%: Ingenol mebutate gel 0.015 % (Picato®) applied on the selected treatment area. Retreatment if the treatment field is not completely cleared of AKs.
195240OG000
Group 2Imiquimod
Arm B: Imiquimod 5% cream applied 3 days per week for 4 weeks to the selected~\> treatment area followed by 4 weeks' rest. Retreatment for another 4 weeks if the treatment field is not completely cleared of AKs at Week 8~\>~\> Imiquimod Cream, 5%: Imiquimod 5% cream applied to the selected treatment area. Retreatment if the treatment field is not completely cleared of AKs
210245OG001

Outcome

Type
SECONDARY
Title
Number of Participants With Partial Clearance of AK Lesions
Description
To compare the partial (at least 75%) clearance of AK lesions in the selected treatment area after the last treatment cycle (at Week 8 or 16)
Time frame
8-16 weeks
Population
Full analysis set: all randomised subjects

Source ClinicalTrials.gov

Trial

Title
Risk of Squamous Cell Carcinoma on Skin Areas Treated With Ingenol Mebutate Gel, 0.015% and Imiquimod Cream, 5%
NCT number
NCT01926496
Phases
PHASE4
Conditions
Actinic Keratosis (AK)
Interventions
Ingenol Mebutate Gel, 0.015%, Imiquimod Cream, 5%
Lead sponsor
LEO Pharma
Results first posted
2020-07-29

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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