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
Cite this record
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
On this page
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.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Mean of Per Subject Percentages of Target Lesions Judged to be Clear (PWA=0) at Visit 8 | Day 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) |
Source ClinicalTrials.gov
Outcomes1
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Mean of Per Subject Percentages of Target Lesions Judged to be Clear (PWA=0) at Visit 8 | Day 106 | Per-Subject Percent of Lesions Clear | MEAN |
Source ClinicalTrials.gov
Results by group3
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Mean of Per Subject Percentages of Target Lesions Judged to be Clear (PWA=0) at Visit 8 | Vehicle | 3.72 | Standard Deviation 10.4 | Per-Subject Percent of Lesions Clear | |
| Mean of Per Subject Percentages of Target Lesions Judged to be Clear (PWA=0) at Visit 8 | A-101 Low Dose | 49.5 | Standard Deviation 36.74 | Per-Subject Percent of Lesions Clear | |
| Mean of Per Subject Percentages of Target Lesions Judged to be Clear (PWA=0) at Visit 8 | A-101 High Dose | 57.88 | Standard Deviation 35.92 | Per-Subject Percent of Lesions Clear |
Source ClinicalTrials.gov
Participant flow9
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Vehicle | 50 | |
| Overall Study | STARTED | A-101 Low Dose | 103 | |
| Overall Study | STARTED | A-101 High Dose | 100 | |
| Overall Study | COMPLETED | Vehicle | 47 | |
| Overall Study | COMPLETED | A-101 Low Dose | 101 | |
| Overall Study | COMPLETED | A-101 High Dose | 92 | |
| Overall Study | NOT COMPLETED | Vehicle | 3 | |
| Overall Study | NOT COMPLETED | A-101 Low Dose | 2 | |
| Overall Study | NOT COMPLETED | A-101 High Dose | 8 |
Source ClinicalTrials.gov
Adverse events201
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | Atrial Fibrillation | Cardiac disorders | Vehicle | 1 | 50 | 1 |
| other | Atrial Fibrillation | Cardiac disorders | A-101 Low Dose | 0 | 103 | 0 |
| other | Atrial Fibrillation | Cardiac disorders | A-101 High Dose | 0 | 100 | 0 |
| other | Bundle Branch Block Left | Cardiac disorders | Vehicle | 0 | 50 | 0 |
| other | Bundle Branch Block Left | Cardiac disorders | A-101 Low Dose | 1 | 103 | 1 |
| other | Bundle Branch Block Left | Cardiac disorders | A-101 High Dose | 0 | 100 | 0 |
| other | Tachycardia | Cardiac disorders | Vehicle | 1 | 50 | 1 |
| other | Tachycardia | Cardiac disorders | A-101 Low Dose | 0 | 103 | 0 |
| other | Tachycardia | Cardiac disorders | A-101 High Dose | 0 | 100 | 0 |
| other | Eyelid Oedema | Eye disorders | Vehicle | 0 | 50 | 0 |
1 to 10 of 201Source ClinicalTrials.gov
See all 201 adverse eventsAdverse event totals9
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Vehicle | 0 | 50 |
| Total, all-cause mortality | A-101 Low Dose | 0 | 103 |
| Total, all-cause mortality | A-101 High Dose | 0 | 100 |
| Total, other adverse events | Vehicle | 11 | 50 |
| Total, other adverse events | A-101 Low Dose | 18 | 103 |
| Total, other adverse events | A-101 High Dose | 26 | 100 |
| Total, serious adverse events | Vehicle | 1 | 50 |
| Total, serious adverse events | A-101 Low Dose | 2 | 103 |
| Total, serious adverse events | A-101 High Dose | 1 | 100 |
Source ClinicalTrials.gov
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.
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