Clinical Trials Directory

Trials / Completed

CompletedNCT00802958

Randomized Study to Compare the Bioavailability of Two Halobetasol Propionate 0.05% Topical Ointments

Bioequivalence of Two Halobetasol Propionate 0.05% Topical Ointments

Status
Completed
Phase
Study type
Observational
Enrollment
76 (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 Halobetasol Propionate 0.05% Ointment in healthy, female subjects.

Conditions

Interventions

TypeNameDescription
DRUGHalobetasol Propionate 0.05% Ointment-Reference ProductSmall amount applied and evaluated over the course of a day
DRUGHalobetasol Propionate 0.05% Ointment-Test ProductSmall amount applied and evaluated over the course of a day

Timeline

Start date
2003-07-01
Primary completion
2003-08-01
Completion
2003-08-01
First posted
2008-12-05
Last updated
2021-10-15

Source: ClinicalTrials.gov record NCT00802958. Inclusion in this directory is not an endorsement.

Randomized Study to Compare the Bioavailability of Two Halobetasol Propionate 0.05% Topical Ointments (NCT00802958) · Clinical Trials Directory