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Trials / Completed

CompletedNCT00803166

Randomized Study to Compare the Bioavailability of Three Halobetasol Propionate 0.05% Topical Creams

Bioequivalence of Three Halobetasol Propionate 0.05% Topical Creams

Status
Completed
Phase
Study type
Observational
Enrollment
60 (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 two test and one reference Halobetasol Propionate 0.05% Cream in healthy, female subjects.

Conditions

Interventions

TypeNameDescription
DRUGHalobetasol Propionate 0.05% Cream-Reference ProductSmall amount applied and evaluated over the course of three days
DRUGHalobetasol Propionate 0.05% Cream-Test product 1Small amount applied and evaluated over the course of three days
DRUGHalobetasol Propionate 0.05% Cream-Test Product 2Small amount applied and evaluated over the course of three days

Timeline

Start date
2004-01-01
Primary completion
2004-01-01
Completion
2004-01-01
First posted
2008-12-05
Last updated
2021-10-18

Source: ClinicalTrials.gov record NCT00803166. Inclusion in this directory is not an endorsement.

Randomized Study to Compare the Bioavailability of Three Halobetasol Propionate 0.05% Topical Creams (NCT00803166) · Clinical Trials Directory