Trials / Completed
CompletedNCT00803218
Randomized Study to Compare the Bioavailability of Two Fluticasone Propionate 0.005% Topical Ointments
Bioequivalence of Two Fluticasone Propionate 0.005% Topical Ointments
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 56 (actual)
- Sponsor
- Padagis LLC · Industry
- Sex
- Female
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study was to compare the relative vasoconstrictive effects of test and reference topical Fluticasone Propionate 0.005% Ointments in healthy, female subjects.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Fluticasone Propionate 0.005% Ointment-Reference Product | Small amount applied and evaluated over the course of one day |
| DRUG | Fluticasone Propionate 0.005% Ointment-Test product | Small amount applied and evaluated over the course of one day |
Timeline
- Start date
- 2002-11-01
- Primary completion
- 2002-11-01
- Completion
- 2002-11-01
- First posted
- 2008-12-05
- Last updated
- 2021-10-15
Source: ClinicalTrials.gov record NCT00803218. Inclusion in this directory is not an endorsement.