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NCT01112787 · ClinicalTrials.gov registry record · Phase 1
A Study to Evaluate the Irritation Potential of Tazarotene Foam on Skin in Healthy Volunteers
A Phase 1 study, sponsored by Stiefel, a GSK Company.
- Completed
- Registry status
- Phase 1
- Development phase
- 39
- Enrollment target
NCT01112787: Completed Phase 1 study, sponsored by Stiefel, a GSK Company.
NCT01112787 is a Phase 1 study that has completed, run by Stiefel, a GSK Company. The registered enrollment target is 39 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (35% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01112787, a Phase 1 study, has completed, sponsored by Stiefel, a GSK Company.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 39 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the irritation level of tazarotene foam after 21 days of exposure on the skin of healthy volunteers.
Primary Outcome
Patch sites will be evaluated for signs of inflammatory skin responses (e.g. erythema, edema, papules) and superficial effects.
Interventions
- DRUG Vehicle Foam
- DRUG Tazarotene Foam
- DRUG Sodium Laural Sulfate
- DRUG Distilled Water
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 39 participants |
| Start Date | 2010-03-26 |
| Est. Completion | 2010-04-26 |
| Phase | Phase 1 |
What the finished NCT01112787 record still lists
NCT01112787 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 39 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (35% lower).
The record links to 0 conditions, and to 4 interventions - of which Vehicle Foam is the first listed.
NCT01112787 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01112787 about?
NCT01112787 is a clinical study titled "A Study to Evaluate the Irritation Potential of Tazarotene Foam on Skin in Healthy Volunteers". The purpose of this study is to evaluate the irritation level of tazarotene foam after 21 days of exposure on the skin of healthy volunteers.
What is the current status of trial NCT01112787?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 39 participants. The study started on 2010-03-26. Estimated completion is 2010-04-26.
What interventions are being tested in trial NCT01112787?
The interventions under investigation include: Vehicle Foam (DRUG), Tazarotene Foam (DRUG), Sodium Laural Sulfate (DRUG), Distilled Water (DRUG).
Who is sponsoring clinical trial NCT01112787?
This trial is sponsored by Stiefel, a GSK Company, which has 37 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01112787's enrollment target sits among peer trials
39 1191st of 2000 higher than 804 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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