Evaluation of Bioavailability of Diclofenac Dermal Products

Status Completed

Clinical Trial Summary

Clinical Trial Description

The study will utilize already FDA-approved marketed diclofenac products in healthy adults to generate data for establishing rate of drug delivery comparisons between diclofenac epolamine patches and diclofenac sodium solution in healthy adults and to determine skin concentrations. This study supports FDA's continuing effort to identify the most accurate, sensitive, reproducible and efficient methods to evaluate topical dermatological drug products. ;

Study Design

Related Conditions & MeSH terms

Bioavailability

Clinical Trial Details

NCT number	NCT03145259
Study type	Interventional
Source	University of Maryland, Baltimore
Contact
Status	Completed
Phase	Early Phase 1
Start date	April 19, 2017
Completion date	May 15, 2020

View Details

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