Last updated on April 2019

Extension Study for the Port Delivery System With Ranibizumab (Portal)


Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Neovascular Age-Related Macular Degeneration
  • Age: Between 50 - 100 Years
  • Gender: Male or Female

Inclusion Criteria:

  • Previous enrollment in and completion of Study GX28228 or Study GR40548, without early treatment or study discontinuation in either study
  • Ability and willingness to undertake all scheduled visits and assessments
  • For women of childbearing potential: agreement to remain abstinent or use contraceptive measures

Exclusion Criteria:

  • Pregnant or breastfeeding, or intending to become pregnant during the treatment period and for at least 28 days after the last intravitreal injection of ranibizumab or 1 year after the last Implant refill of ranibizumab
  • History of other ocular diseases that give reasonable suspicion of a disease or condition that contraindicates the use of ranibizumab, that might affect interpretation of the results of the study or that renders the participant at high risk for treatment complications
  • History of other diseases, metabolic dysfunction, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of ranibizumab or placement of the Implant and that might affect interpretation of the results of the study or that renders the participant at high risk of treatment complications
  • Requirement for continuous use of any medications or treatments indicated in the "Prohibited Therapy"

Recruitment Status: Open


Brief Description Eligibility Contact Research Team


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