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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00354445
Other study ID # EOP1023
Secondary ID
Status Recruiting
Phase Phase 4
First received July 18, 2006
Last updated January 12, 2007
Start date June 2006

Study information

Verified date January 2007
Source Eyetech Pharmaceuticals
Contact Macugen Information
Phone 1-866-622-8436
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to explore the safety and efficacy of Macugen given as maintenance therapy in patients who have had initial success with another AMD treatment. Patients must have 1, but not more than 3 prior treatments for Neovascular AMD.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 50 Years and older
Eligibility Inclusion Criteria:

- Subfoveal CNV secondary to AMD

- At least 1 but not more than 3 prior treatments for AMD

Exclusion Criteria:

- Subfoveal scar or subfoveal atrophy

- Significant media opacities, including cataract, which might interfere with visual acuity

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
pegaptanib sodium (Macugen)


Locations

Country Name City State
United States Retina Research Institute of Texas, LLC Abilene Texas

Sponsors (2)

Lead Sponsor Collaborator
Eyetech Pharmaceuticals Pfizer

Country where clinical trial is conducted

United States, 

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