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NCT00865267 · ClinicalTrials.gov registry record · Phase 1
The Dose-response Study of Topically Delivered Halobetasol Propionate Ointment in Normal Skin in Healthy Adult Subjects
A Phase 1 study, sponsored by Actavis.
- Completed
- Registry status
- Phase 1
- Development phase
- 20
- Enrollment target
NCT00865267: Completed Phase 1 study, sponsored by Actavis.
NCT00865267 is a Phase 1 study that has completed, run by Actavis. The registered enrollment target is 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00865267, a Phase 1 study, has completed, sponsored by Actavis.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 20 participants
- Enrollment target
Study Summary
The purpose of this study is to determine the duration of application of halobetasol propionate 0.05% ointment to be used in a definitive study of bioequivalence of to formulations of this ointment. Part A: To validate vasoconstrictor assay precision. Part B: To evaluate the dose response vasoconstriction profile of Ultravate® 0.05% ointment at different dose durations over a short period of time (0.17 - 4 hrs).
Interventions
- DRUG Ultravate® 0.05% ointment, single exposure
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2003-12 |
| Est. Completion | 2003-12 |
| Phase | Phase 1 |
What the finished NCT00865267 record still lists
NCT00865267 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).
The record links to 0 conditions, and to 1 intervention - of which Ultravate® 0.05% ointment, single exposure is the first listed.
NCT00865267 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00865267 about?
NCT00865267 is a clinical study titled "The Dose-response Study of Topically Delivered Halobetasol Propionate Ointment in Normal Skin in Healthy Adult Subjects". The purpose of this study is to determine the duration of application of halobetasol propionate 0.05% ointment to be used in a definitive study of bioequivalence of to formulations of this ointment. Part A: To validate vasoconstrictor assay precision. Part B: To evaluate the dose response vasocons...
What is the current status of trial NCT00865267?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2003-12. Estimated completion is 2003-12.
What interventions are being tested in trial NCT00865267?
The interventions under investigation include: Ultravate® 0.05% ointment, single exposure (DRUG).
Who is sponsoring clinical trial NCT00865267?
This trial is sponsored by Actavis, which has 79 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00865267's enrollment target sits among peer trials
20 1629th of 2000 higher than 285 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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