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

Sponsor
Control Delivery Systems (Industry)
Overall Status
Unknown status
CT.gov ID
NCT00032396
Collaborator
Bausch & Lomb Incorporated (Industry)
1

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Drug: Retisert Implant
Phase 2

Study Design

Study Type:
Interventional
Primary Purpose:
Treatment
Study Start Date :
Nov 1, 2001

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    55 Years to 0 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Control Delivery Systems, Inc. Watertown Massachusetts United States 02472

    Sponsors and Collaborators

    • Control Delivery Systems
    • Bausch & Lomb Incorporated

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00032396
    Other Study ID Numbers:
    • CDS FL-004
    First Posted:
    Mar 22, 2002
    Last Update Posted:
    May 29, 2006
    Last Verified:
    Dec 1, 2002

    Study Results

    No Results Posted as of May 29, 2006