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Comparison · NCT02556788-sae

CD5789 (Trifarotene) 50µg/g Cream vs Placebo 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. CD5789 (Trifarotene) 50µg/g Cream vs Placebo Cream: serious adverse events. Trial comparisons, record NCT02556788-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02556788-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 10.003320.0009120.012wilson
Risk in group 20.006560.002550.0167wilson
Risk difference, group 1 minus group 2-0.00324-0.01370.00635newcombe hybrid score
Risk ratio, group 1 over group 20.5070.09312.76log
Odds ratio, group 1 over group 20.5050.09222.77log
Number needed to treat, for one fewer participant with a serious adverse event on CD5789 (Trifarotene) 50µg/g Cream than on Placebo Cream309from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1CD5789 (Trifarotene) 50µg/g CreamCD5789 (Trifarotene) 50µg/g cream applied once daily during 12 weeks.2602EG000
Group 2Placebo CreamPlacebo cream applied once daily during 12 weeks.4610EG001

Harm

What it counts
Total, serious adverse events
Time frame
Each participant's adverse events were collected starting at the first visit (screening) until the last visit (Week 12).

Source ClinicalTrials.gov

Trial

Title
Double-Blind Efficacy and Safety of CD5789 (Trifarotene) 50µg/g Cream Versus Vehicle Cream in Acne Vulgaris
NCT number
NCT02556788
Phases
PHASE3
Conditions
Acne Vulgaris
Interventions
CD5789 (trifarotene) 50µg/g Cream, Placebo Cream
Lead sponsor
Galderma R&D
Results first posted
2019-09-03

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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