At a glance
ClinicalIndex Comparison RecordEarly Ph 1Completed· 12 enrolled
Drug / intervention
Diclofenac Epolamine Patch +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Evaluation of Bioavailability of Diclofenac Dermal Products
In Brief
A Early Phase 1 clinical trial evaluating Diclofenac Epolamine Patch and diclofenac sodium solution for Bioavailability. Completed, enrolled 12 participants across 1 site.
Detailed Summary
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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsBioavailability
CountriesUnited States
CollaboratorsFood and Drug Administration (FDA)
Timeline
Early Ph 1CompletedFinished
201820192020202120222023202420252026
Enrollment StartApr 2017
First PostedMay 2017
Primary CompletionAug 2019
Study CompletionMay 2020
TodayJul 2026
First PostedMay 9, 2017
Enrollment StartApr 19, 2017
Primary CompletionAug 29, 2019
Study CompletionMay 15, 2020
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 9.1 years ago
Interventions
Diclofenac Epolamine Patchdrug
patch
diclofenac sodium solutiondrug
solution