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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 is a Phase 1 study that has completed, run by Actavis. The registered enrollment target is 20 participants.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00865267
The ClinicalTrials.gov registry entry for NCT00865267 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Actavis, which has 79 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Ultravate® 0.05% ointment, single exposure is the first listed.
NCT00865267 reports 0 study locations.
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.
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