Phase II Study of AP0302 5% Versus a Vehicle Comparator

Status Completed

Clinical Trial Summary

This study is designed to evaluate the analgesic safety and efficacy of study drug (AP0302) applied topically every 6 hours as compared to a vehicle, in subjects experiencing delayed onset muscle soreness.

Clinical Trial Description

The purpose of this study is to evaluate the efficacy and safety of S-Ibuprofen Topical Gel 5% in reducing pain/soreness associated with delayed onset muscle soreness (DOMS). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02324985
Study type	Interventional
Source	Aponia Laboratories, Inc.
Contact
Status	Completed
Phase	Phase 2
Start date	January 2015
Completion date	June 2016

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