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Trial · NCT03148691

A Randomized, Vehicle-Controlled Study of 2 Concentrations of A-101 for the Treatment of Seborrheic Keratosis

NCT03148691, Phase 2, Completed, Aclaris Therapeutics, Inc.; results first posted 2019-05-06

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. A Randomized, Vehicle-Controlled Study of 2 Concentrations of A-101 for the Treatment of Seborrheic Keratosis. Trials, record NCT03148691. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03148691

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Trial

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

Title
A Randomized, Vehicle-Controlled Study of 2 Concentrations of A-101 for the Treatment of Seborrheic Keratosis
NCT number
NCT03148691
Status
Completed
Phases
Phase 2
Enrollment
253 participants, actual
Lead sponsor
Aclaris Therapeutics, Inc.
Conditions
Seborrheic Keratosis
Interventions
A-101
First posted
2017-05-11
Last updated
2019-05-06
Results first posted
2019-05-06

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryMean of Per Subject Percentages of Target Lesions Judged to be Clear (PWA=0) at Visit 8Day 106
Mean of per subject percentages of target lesions judged to be clear (PWA=0) at Visit 8 Grade Descriptor 0 Clear: no visible seborrheic keratosis lesion 1. Near Clear: a visible seborrheic keratosis lesion with a surface appearance different from the surrounding skin (not elevated) 2. Thin: a visible seborrheic keratosis lesion (thickness ≤ 1 mm) 3. Thick: a visible seborrheic keratosis lesion (thickness \> 1 mm)

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMean of Per Subject Percentages of Target Lesions Judged to be Clear (PWA=0) at Visit 8Day 106Per-Subject Percent of Lesions ClearMEAN

Results by group3

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

OutcomeGroupCategoryValueSpreadUnits
Mean of Per Subject Percentages of Target Lesions Judged to be Clear (PWA=0) at Visit 8Vehicle3.72Standard Deviation 10.4Per-Subject Percent of Lesions Clear
Mean of Per Subject Percentages of Target Lesions Judged to be Clear (PWA=0) at Visit 8A-101 Low Dose49.5Standard Deviation 36.74Per-Subject Percent of Lesions Clear
Mean of Per Subject Percentages of Target Lesions Judged to be Clear (PWA=0) at Visit 8A-101 High Dose57.88Standard Deviation 35.92Per-Subject Percent of Lesions Clear

Participant flow9

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDVehicle50
Overall StudySTARTEDA-101 Low Dose103
Overall StudySTARTEDA-101 High Dose100
Overall StudyCOMPLETEDVehicle47
Overall StudyCOMPLETEDA-101 Low Dose101
Overall StudyCOMPLETEDA-101 High Dose92
Overall StudyNOT COMPLETEDVehicle3
Overall StudyNOT COMPLETEDA-101 Low Dose2
Overall StudyNOT COMPLETEDA-101 High Dose8

Adverse events201

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAtrial FibrillationCardiac disordersVehicle1501
otherAtrial FibrillationCardiac disordersA-101 Low Dose01030
otherAtrial FibrillationCardiac disordersA-101 High Dose01000
otherBundle Branch Block LeftCardiac disordersVehicle0500
otherBundle Branch Block LeftCardiac disordersA-101 Low Dose11031
otherBundle Branch Block LeftCardiac disordersA-101 High Dose01000
otherTachycardiaCardiac disordersVehicle1501
otherTachycardiaCardiac disordersA-101 Low Dose01030
otherTachycardiaCardiac disordersA-101 High Dose01000
otherEyelid OedemaEye disordersVehicle0500

Adverse event totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityVehicle050
Total, all-cause mortalityA-101 Low Dose0103
Total, all-cause mortalityA-101 High Dose0100
Total, other adverse eventsVehicle1150
Total, other adverse eventsA-101 Low Dose18103
Total, other adverse eventsA-101 High Dose26100
Total, serious adverse eventsVehicle150
Total, serious adverse eventsA-101 Low Dose2103
Total, serious adverse eventsA-101 High Dose1100

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 comparisons0

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

None in this release.

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/NCT03148691

GET https://conductscience.org/api/trials/v1/NCT03148691/events?page=2