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NCT00032396 Clinical Trial

A Study to Evaluate Retisert in the Treatment of Patients With the "Wet" Form of Age-Related Macular Degeneration

Macular Degeneration Clinical Trial

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00032396
Other study ID # CDS FL-004
Secondary ID
Status Active, not recruiting
Phase Phase 2
First received March 20, 2002
Last updated May 25, 2006
Start date November 2001

Study information
Verified date December 2002
Source Control Delivery Systems
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

A study evaluating Retisert in patients with age-related macular degeneration

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 55 Years and older
Eligibility

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Retisert Implant

Locations
Country Name City State
United States Control Delivery Systems, Inc. Watertown Massachusetts

Sponsors (2)
Lead Sponsor Collaborator
Control Delivery Systems Bausch & Lomb Incorporated

Country where clinical trial is conducted

United States, 

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