Status:

COMPLETED

Anecortave Acetate in Patients With Exudative Age-related Macular Degeneration (AMD)

Lead Sponsor:

Alcon Research

Conditions:

Macular Degeneration

Eligibility:

All Genders

50+ years

Phase:

PHASE3

Brief Summary

The purpose of this study was to evaluate the effect of the dose concentration and administration frequency of Anecortave Acetate (AA) on visual acuity (VA) and lesion size when administered by poster...

Eligibility Criteria

Inclusion

  • Clinical diagnosis of exudative AMD and a primary or recurrent (after laser photocoagulation) subfoveal choroidal neovascularization (CNV) lesion.
  • Other protocol-defined inclusion criteria may apply.

Exclusion

  • Less than 50 years of age.
  • Other protocol-defined exclusion criteria may apply.

Key Trial Info

Start Date :

March 1 2005

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 1 2008

Estimated Enrollment :

240 Patients enrolled

Trial Details

Trial ID

NCT00299507

Start Date

March 1 2005

End Date

April 1 2008

Last Update

November 28 2012

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Alcon Study Sites

Fort Worth, Texas, United States, 76134