Pasadena, California 91105


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.

Study summary:

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).


Inclusion Criteria: - no clinically significant medical conditions - BMI between 18-30 - negative drug, alcohol, pregnancy screens - other protocol-defined inclusion criteria may apply Exclusion Criteria: - no upper extremity workout in last 6 months - no job requiring heavy lifting - history of muscle disorders - allergy or intolerance to study drug - history of recent pain medication use - other protocol-defined exclusion criteria may apply



Primary Contact:

Principal Investigator
Sonia Singla, DO
Lotus Clinical Research

Kenneth M Corroon, Chief Executive Officer

Backup Contact:


Location Contact:

Pasadena, California 91105
United States

There is no listed contact information for this specific location.

Site Status: Recruiting

Data Source:

Date Processed: June 25, 2018

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