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Phase 3 Study to evaluate Anecortave Acetate vs. Visudyne for the treatment of the wet form of AMD.



Phase 3 Study to evaluate Anecortave Acetate vs. Visudyne for the treatment of the wet form of AMD.

For Condition: Macular Degeneration
Status: No longer recruiting
Sponsor(s): Alcon Research ,
Synopsis: The purpose of this study is to demonstrate that Anecortave Acetate is as effective after twelve months of treatment as photodynamic therapy (PDT) with Visudyne in patients eligible for initial PDT treatment for wet age-related macular degeneration.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Active Control, Single Group Assignment, Safety/Efficacy Study
Minimum Age/Maximum Age: 50 Years/
Genders: Both
Protocol Entry Criteria: Patients of any race, either gender, aged 50 years and above, diagnosed with subfoveal CNV due to AMD with best corrected logMAR visual acuity of 20/40 (snellen equivalent) to 20/400 (Snellen equivalent) in the study eye. Clinically relevant concomitant diseases will be excluded.
Total Enrollment: 

Location and Contact Information:

US, Canada, Australia and Europe
Ft. Worth,  Texas, 
United States
 


Additional Information:
Study ID Numbers:
  C-01-99; 
Study Start Date: 
Record last reviewed: September 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00041483

Other Macular Degeneration Studies:
1. Randomized Trials of Vitamin Supplements and Eye Disease

2. Randomized Trial of Beta-Carotene and Macular Degeneration

3. Rheopheresis Blood Filtration Study for the Treatment of Dry Age-Related Macular Degeneration (AMD)

4. Genetic Factors in Age-Related Macular Degeneration

5. Complications of Age-Related Macular Degeneration Prevention Trial (CAPT)

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Phase 3 Study to evaluate Anecortave Acetate vs. Visudyne for the treatment of the wet form of AMD.

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