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Trial · NCT02556788

Double-Blind Efficacy and Safety of CD5789 (Trifarotene) 50µg/g Cream Versus Vehicle Cream in Acne Vulgaris

NCT02556788, Phase 3, Completed, Galderma R&D; results first posted 2019-09-03

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Double-Blind Efficacy and Safety of CD5789 (Trifarotene) 50µg/g Cream Versus Vehicle Cream in Acne Vulgaris. Trials, record NCT02556788. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02556788

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Double-Blind Efficacy and Safety of CD5789 (Trifarotene) 50µg/g Cream Versus Vehicle Cream in Acne Vulgaris
NCT number
NCT02556788
Status
Completed
Phases
Phase 3
Enrollment
1,212 participants, actual
Lead sponsor
Galderma R&D
Conditions
Acne Vulgaris
Interventions
CD5789 (trifarotene) 50µg/g Cream, Placebo Cream
First posted
2015-09-22
Last updated
2019-11-12
Results first posted
2019-09-03

Source ClinicalTrials.gov

Registered outcomes1

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryInvestigator Global Assessment (IGA) Score of 1 (Almost Clear) or 0 (Clear)From Baseline to Week 12Number of subjects who achieved an Investigator Global Assessment (IGA) score of 1 (almost clear) or 0 (Clear) and at least a 2-grade improvement from Baseline to Week 12.

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYInvestigator Global Assessment (IGA) Score of 1 (Almost Clear) or 0 (Clear)From Baseline to Week 12ParticipantsCOUNT_OF_PARTICIPANTS

Results by group2

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Investigator Global Assessment (IGA) Score of 1 (Almost Clear) or 0 (Clear)CD5789 (Trifarotene) 50µg/g Cream255Participants
Investigator Global Assessment (IGA) Score of 1 (Almost Clear) or 0 (Clear)Placebo Cream157Participants

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDCD5789 (Trifarotene) 50µg/g Cream602
Overall StudySTARTEDPlacebo Cream610
Overall StudyCOMPLETEDCD5789 (Trifarotene) 50µg/g Cream558
Overall StudyCOMPLETEDPlacebo Cream573
Overall StudyNOT COMPLETEDCD5789 (Trifarotene) 50µg/g Cream44
Overall StudyNOT COMPLETEDPlacebo Cream37

Adverse events52

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherSunburnInjury, poisoning and procedural complicationsCD5789 (Trifarotene) 50µg/g Cream2602
otherSunburnInjury, poisoning and procedural complicationsPlacebo Cream0610
otherDrug Administered at Inappropriate SiteInjury, poisoning and procedural complicationsCD5789 (Trifarotene) 50µg/g Cream1602
otherDrug Administered at Inappropriate SiteInjury, poisoning and procedural complicationsPlacebo Cream0610
otherBlood Bilirubin IncreasedInvestigationsCD5789 (Trifarotene) 50µg/g Cream0602
otherBlood Bilirubin IncreasedInvestigationsPlacebo Cream1610
otherBlood Creatinine IncreasedInvestigationsCD5789 (Trifarotene) 50µg/g Cream0602
otherBlood Creatinine IncreasedInvestigationsPlacebo Cream1610
otherLymphadenopathyBlood and lymphatic system disordersCD5789 (Trifarotene) 50µg/g Cream1602
otherLymphadenopathyBlood and lymphatic system disordersPlacebo Cream0610

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityCD5789 (Trifarotene) 50µg/g Cream0602
Total, all-cause mortalityPlacebo Cream0610
Total, other adverse eventsCD5789 (Trifarotene) 50µg/g Cream21602
Total, other adverse eventsPlacebo Cream5610
Total, serious adverse eventsCD5789 (Trifarotene) 50µg/g Cream2602
Total, serious adverse eventsPlacebo Cream4610

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons3

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
CD5789 (Trifarotene) 50µg/g Cream vs Placebo Cream: Investigator Global Assessment (IGA) Score of 1 (Almost Clear) or 0 (Clear)Trial comparisons
CD5789 (Trifarotene) 50µg/g Cream vs Placebo Cream: deaths from any causeTrial comparisons
CD5789 (Trifarotene) 50µg/g Cream vs Placebo Cream: serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02556788

GET https://conductscience.org/api/trials/v1/NCT02556788/events?page=2