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Clinical Study for the Treatment of Adhesive Capsulitis of the Shoulder — AC  

Adhesive Capsulitis Clinical Trial

Official title:
A Randomized, Double-blind, Placebo-controlled Study of the Safety and Efficacy of AA4500 for the Treatment of Adhesive Capsulitis of the Shoulder

Clinical Trial Summary

The objectives of this study are to assess the safety, effectiveness, and immunogenicity of AA4500 in the treatment of adhesive capsulitis.

Clinical Trial Description

Study is a Phase 2b, double-blind, placebo-controlled study of the safety and efficacy of AA4500 for the treatment of adhesive capsulitis of the shoulder. To be eligible for treatment, a subject must have unilateral idiopathic adhesive capsulitis of the shoulder with restricted range of motion in the affected shoulder for at least 3 months but not more than 12 months. Subjects will be screened for study eligibility within 28 days before injection of study drug.

Approximately 300 adult women and men are to be enrolled in this study. Following screening and determination of study eligibility, subjects will be randomized 3:1 to receive 0.58 mg of AA4500 or placebo. Subjects will receive up to 3 injections of study drug. Each injection will be separated by a minimum of 21 days. Subjects will also be instructed in home shoulder exercises after the first injection. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02006719
Study type Interventional
Source Endo Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date November 2013
Completion date December 2014
View Details
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