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Trial · NCT02667236

A Study of A-101 Solution 40% in Subjects With Seborrheic Keratosis.

NCT02667236, Phase 3, Completed, Aclaris Therapeutics, Inc.; results first posted 2017-11-13

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. A Study of A-101 Solution 40% in Subjects With Seborrheic Keratosis. Trials, record NCT02667236. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02667236

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Trial

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

Title
A Study of A-101 Solution 40% in Subjects With Seborrheic Keratosis.
NCT number
NCT02667236
Status
Completed
Phases
Phase 3
Enrollment
450 participants, actual
Lead sponsor
Aclaris Therapeutics, Inc.
Conditions
Seborrheic Keratosis
Interventions
A-101 Solution, Vehicle Solution
First posted
2016-01-28
Last updated
2018-02-06
Results first posted
2017-11-13

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryProportion of Subjects With Target Lesion Clearance as Assessed by the Physician Lesion AssessmentDay 106 of the study
Proportion of subjects for whom all target lesions were judged to be clear on the Physician Lesion Assessment Scale (PLA=0) at Visit 8. The PLA Scale is a 4 point scale used by the investigator to assess each subject's target SK Lesion.
SecondaryProportion of Subjects With 3 of 4 Target Lesion ClearanceDay 106 of the studyProportion of Subjects for whom at least 3 of 4 target lesions were judged to be clear on the Physician Lesion Assessment (PLA=0) at Visit 8

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYProportion of Subjects With Target Lesion Clearance as Assessed by the Physician Lesion AssessmentDay 106 of the studyITT Population; all randomized subjectsParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYProportion of Subjects With 3 of 4 Target Lesion ClearanceDay 106 of the studyITT population; all randomized subjectsParticipantsCOUNT_OF_PARTICIPANTS

Results by group4

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

OutcomeGroupCategoryValueSpreadUnits
Proportion of Subjects With Target Lesion Clearance as Assessed by the Physician Lesion AssessmentA-101 Solution9Participants
Proportion of Subjects With Target Lesion Clearance as Assessed by the Physician Lesion AssessmentVehicle Solution0Participants
Proportion of Subjects With 3 of 4 Target Lesion ClearanceA-101 Solution30Participants
Proportion of Subjects With 3 of 4 Target Lesion ClearanceVehicle Solution0Participants

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDA-101 Solution223
Overall StudySTARTEDVehicle Solution227
Overall StudyCOMPLETEDA-101 Solution220
Overall StudyCOMPLETEDVehicle Solution226
Overall StudyNOT COMPLETEDA-101 Solution3
Overall StudyNOT COMPLETEDVehicle Solution1

Adverse events30

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherNasopharyngitisInfections and infestationsA-101 Solution32233
otherNasopharyngitisInfections and infestationsVehicle Solution72277
otherBronchitisInfections and infestationsA-101 Solution32233
otherBronchitisInfections and infestationsVehicle Solution12271
otherUpper Respiratory InfectionInfections and infestationsA-101 Solution12231
otherUpper Respiratory InfectionInfections and infestationsVehicle Solution32273
otherActinic KeratosisSkin and subcutaneous tissue disordersA-101 Solution32233
otherActinic KeratosisSkin and subcutaneous tissue disordersVehicle Solution02270
otherSeasonal AllergyImmune system disordersA-101 Solution02230
otherSeasonal AllergyImmune system disordersVehicle Solution42274

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityA-101 Solution0223
Total, all-cause mortalityVehicle Solution0227
Total, other adverse eventsA-101 Solution10223
Total, other adverse eventsVehicle Solution14227
Total, serious adverse eventsA-101 Solution4223
Total, serious adverse eventsVehicle Solution6227

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
30365590DERIVED

Source PubMed

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 comparisons4

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

ComparisonSource
A-101 Solution vs Vehicle Solution: Proportion of Subjects With 3 of 4 Target Lesion ClearanceTrial comparisons
A-101 Solution vs Vehicle Solution: deaths from any causeTrial comparisons
A-101 Solution vs Vehicle Solution: Proportion of Subjects With Target Lesion Clearance as Assessed by the Physician Lesion AssessmentTrial comparisons
A-101 Solution vs Vehicle Solution: 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/NCT02667236

GET https://conductscience.org/api/trials/v1/NCT02667236/events?page=2