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Suprachoroidal Injection of CLS-TA in Patients With Non-infectious Uveitis — AZALEA  

Uveitis Clinical Trial

Official title:
Open-label Safety Study of Suprachoroidal Triamcinolone Acetonide Injectable Suspension in Patients With Non-Infectious Uveitis

Clinical Trial Summary

This open-label study is designed to evaluate the safety of suprachoroidally administered triamcinolone acetone injectable suspension, CLS-TA, in patients with non-infectious uveitis with and without macular edema.

Clinical Trial Description

This is a Phase 3, open-label multicenter study to assess the safety of 4 mg of CLS-TA administered via suprachoroidal injection in the treatment of patients diagnosed with noninfectious uveitis with and without macular edema. Qualified patients will be enrolled and receive two suprachoroidal injections of CLS-TA administered to the study eye approximately 12 weeks apart (Visit 2 and Visit 5). Follow-up visits will be conducted monthly up to 24 weeks (Visit 8). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03097315
Study type Interventional
Source Clearside Biomedical, Inc.
Contact
Status Completed
Phase Phase 3
Start date April 4, 2017
Completion date January 24, 2018
View Details
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