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

NCT ID: NCT00032396

Last Updated: 2006-05-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE2

Study Classification

INTERVENTIONAL

Study Start Date

2001-11-30

Brief Summary

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

Detailed Description

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Conditions

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Macular Degeneration

Keywords

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AMD ARMD Age-Related Macular Degeneration Subfoveal Choroidal Neovascularization CNV

Study Design

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Primary Study Purpose

TREATMENT

Interventions

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Retisert Implant

Intervention Type DRUG

Eligibility Criteria

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Minimum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bausch & Lomb Incorporated

INDUSTRY

Sponsor Role collaborator

Control Delivery Systems

INDUSTRY

Sponsor Role lead

Locations

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Control Delivery Systems, Inc.

Watertown, Massachusetts, United States

Site Status

Countries

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United States

Other Identifiers

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CDS FL-004

Identifier Type: -

Identifier Source: org_study_id