Expired Study
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Pasadena, California 91105


Purpose:

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).


Criteria:

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


NCT ID:

NCT02324985


Primary Contact:

Principal Investigator
Sonia Singla, DO
Lotus Clinical Research


Backup Contact:

N/A


Location Contact:

Pasadena, California 91105
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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