Not currently recruiting at UCSF

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

a study on Macular Degeneration

Summary

for people ages 50 years and up (full criteria)
at San Francisco, California and other locations
study started
estimated completion

Description

Summary

This study will evaluate the long-term safety and tolerability of the Port Delivery System (PDS) with ranibizumab 100 mg/mL with refills administered every 24 weeks (Q24W) for approximately 144 weeks in participants with neovascular age-related macular degeneration (nAMD) who have completed either Phase II Study GX28228 or Phase III Study GR40548.

Official Title

A Multicenter, Open-Label Extension Study to Evaluate the Long-Term Safety and Tolerability of the Port Delivery System With Ranibizumab in Patients With Neovascular Age-Related Macular Degeneration

Keywords

Neovascular Age-Related Macular DegenerationMacular DegenerationWet Macular DegenerationRanibizumabPDS Implant with Ranibizumab 100 mg/mL

Eligibility

You can join if…

Open to people ages 50 years and up

  • 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

You CAN'T join if...

  • 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"

Locations

  • UCSF; Ophthalmology in progress, not accepting new patients
    San FranciscoCalifornia94143United States
  • West Coast Retina Medical Group in progress, not accepting new patients
    San FranciscoCalifornia94109United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Hoffmann-La Roche
ID
NCT03683251
Phase
Phase 3
Study Type
Interventional
Last Updated