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Irritation and Sensitization Study of HP-5000 Topical System

Osteoarthritis of the Knee Clinical Trial

Official title:
An Evaluator-blinded, Randomized Within-subject Repeat Insult Study to Evaluate Potential Skin Irritation and Sensitization of HP-5000 (Diclofenac Sodium Topical System) in Healthy Adults

Clinical Trial Summary

This study will assess skin irritation and sensitization for HP-5000 patch in healthy subjects.

Clinical Trial Description

This is an evaluator-blinded, randomized phase 1 study evaluating skin irritation and sensitization of HP-5000 topical system in comparison to control patches. The study will consist of a 4-week Screening Phase and a Treatment Phase. The Treatment Phase will consist of the following periods: an Induction Period, a Rest Period followed by a Challenge Period and if needed, a Re-Challenge Period. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04882319
Study type Interventional
Source Noven Therapeutics
Contact
Status Completed
Phase Phase 1
Start date June 3, 2021
Completion date March 11, 2022
View Details
See also
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