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Randomized Study to Compare the Bioequivalence of Two Fluticasone Propionate 0.05% Topical Creams

NCT00803465 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 115

Last updated 2021-10-18

No results posted yet for this study

Summary

The purpose of this study was to compare the relative vasoconstrictive effects of test and reference topical Fluticasone Propionate 0.05% Cream in healthy, female subjects.

Conditions

  • Healthy

Interventions

DRUG

Fluticasone Propionate 0.05% Cream-Reference Product

Small amount applied and evaluated over the course of two days

DRUG

Fluticasone Propionate 0.05% Cream-Test product

Small amount applied and evaluated over the course of two days

Sponsors & Collaborators

  • Padagis LLC

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2003-04-30
Primary Completion
2003-06-30
Completion
2003-06-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00803465 on ClinicalTrials.gov