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Comparison · NCT04773587-sae

Roflumilast Cream 0.15% vs Vehicle Cream: serious adverse events

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. Roflumilast Cream 0.15% vs Vehicle Cream: serious adverse events. Trial comparisons, record NCT04773587-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04773587-sae

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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 10.009240.00360.0235wilson
Risk in group 2000.0171wilson
Risk difference, group 1 minus group 20.00924-0.008750.0235newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to harm, for one more participant with a serious adverse event on Roflumilast Cream 0.15% than on Vehicle Cream108from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: vehicle.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Roflumilast Cream 0.15%Participants with mild to moderate AD applied roflumilast cream 0.15% once daily (QD) for 4 weeks.4433EG000
Group 2Vehicle CreamParticipants with mild to moderate AD applied vehicle cream QD for 4 weeks.0221EG001

Harm

What it counts
Total, serious adverse events
Time frame
Up to approximately 29 days

Source ClinicalTrials.gov

Trial

Title
Trial of PDE4 Inhibition With Roflumilast for the Management of Atopic Dermatitis
NCT number
NCT04773587
Phases
PHASE3
Conditions
Atopic Dermatitis Eczema
Interventions
Roflumilast Cream 0.15%, Vehicle Cream
Lead sponsor
Arcutis Biotherapeutics, Inc.
Results first posted
2024-10-09

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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