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Comparison · NCT01555463-sae

Azelaic Acid Foam, 15% (BAY39-6251) vs Vehicle Foam: 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. Azelaic Acid Foam, 15% (BAY39-6251) vs Vehicle Foam: serious adverse events. Trial comparisons, record NCT01555463-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01555463-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 10.006210.002110.0181wilson
Risk in group 20.008370.003260.0213wilson
Risk difference, group 1 minus group 2-0.00216-0.01570.0108newcombe hybrid score
Risk ratio, group 1 over group 20.7420.1673.3log
Odds ratio, group 1 over group 20.7410.1653.33log
Number needed to treat, for one fewer participant with a serious adverse event on Azelaic Acid Foam, 15% (BAY39-6251) than on Vehicle Foam464from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: vehicle.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Azelaic Acid Foam, 15% (BAY39-6251)0.5 g azelaic acid (AzA) foam, 15% applied twice daily (BID) topical and nonocclusive on facial skin for 12 weeks.3483EG000
Group 2Vehicle Foam0.5 g vehicle foam applied twice daily topical and nonocclusive on facial skin for 12 weeks.4478EG001

Harm

What it counts
Total, serious adverse events
Time frame
From start of treatment until end of study.

Source ClinicalTrials.gov

Trial

Title
Safety and Efficacy of Azelaic Acid Foam, 15 % in Papulopustular Rosacea
NCT number
NCT01555463
Phases
PHASE3
Conditions
Papulopustular Rosacea
Interventions
Azelaic acid foam, 15% (BAY39-6251), Vehicle foam
Lead sponsor
LEO Pharma
Results first posted
2015-01-27

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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