A Safety and Efficacy Study of Abicipar Pegol in Participants With Neovascular Age-related Macular Degeneration

Study Identifier
150998-005
CT.gov Identifier
NCT02462928
EudraCT Identifier
2014-004579-22
EUCTIS ID
Not available
For general inquiries, please contact

844-663-3742 or [email protected]

Study Complete

Results Available

Statistical Analysis Plan
Available Language(s): English
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Protocol
Available Language(s): English
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Study Details

Medical Condition
  • Macular Degeneration - Other
    • Study Drug
  • Abicipar Pegol
  • Ranibizumab
    • Phase
    Phase 3
    Sex
    Female & Male
    Age
    50+ years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Diagnosis of age-related macular degeneration in at least 1 eye * Best corrected visual acuity of 20/40 to 20/320 in the study eye * Best corrected visual acuity of 20/200 or better in the non-study eye
    Exclusion Criteria:
    * History of vitrectomy, macular surgery, or glaucoma surgery in the study eye * Cataract or refractive surgery in the study eye within the last 3 months

    Protocol Summary

    This is a safety and efficacy study of abicipar pegol in participants with neovascular age-related macular degeneration.

    Study Locations

    Location
    Status
    Location
    Retinal Research Institute, LLC
    Phoenix, Arizona, United States, 85014
    Status
    Not applicable
    Location
    Associated Retina Consultants, Ltd.
    Phoenix, Arizona, United States, 85020
    Status
    Not applicable
    Location
    Arizona Retina and Vitreous Consultants
    Phoenix, Arizona, United States, 85021
    Status
    Not applicable
    Location
    Retina Associates Southwest, P.C.
    Tucson, Arizona, United States, 85710
    Status
    Not applicable
    Location
    The Retina Partners
    Encino, California, United States, 91436
    Status
    Not applicable
    Location
    Retina Consultants of Orange County
    Fullerton, California, United States, 92835
    Status
    Not applicable
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