Long-Term Follow Up of VOY-101 for Non-Neovascular Age-Related Macular Degeneration

This study is a long-term follow-up for people who previously received an injection of VOY-101 for advanced non-neovascular age-related macular degeneration (AMD). This is an observational study, meaning you won't receive any new treatments as part of this study. Researchers want to understand the long-term safety of VOY-101 by tracking any side effects related to the eye or body for up to 3 years. To join, you must have previously participated in a VOY-101 study (PBI-AMD-001 or PBI-AMD-002). The current status of this study is unclear, and it plans to enroll 88 participants.

Study design
This is an observational study, meaning no new treatments are given. It is a long-term follow-up for people who previously received VOY-101, with a planned enrollment of 88 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for 3 years to track the frequency of side effects related to VOY-101.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07660640

Long-Term Follow Up of VOY-101 Non-nAMD Extension Study

Enrolling by Invitation
Not specifiedAges 50+Observational
Perceive Biotherapeutics, Inc.
~88 participants
Updated 2026-06-22 on ClinicalTrials.gov
What's tested:observational studyVOY-101

At a glance

Recruiting sites
0 of 4 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Frequency of ocular and systemic VOY-101 related AEs
Measured over 3 years
Age-Related Macular Degeneration (AMD)
Non-Neovascular Age-Related Macular Degeneration
4 sites across 4 states
Massachusetts1
Texas1
Utah1
Israel1

This trial hasn't published a contact. View it on ClinicalTrials.gov

  • Frequency of ocular and systemic VOY-101 related AEs3 years

    Frequency of ocular and systemic VOY-101 related AEs (serious \[SAEs\] and treatment-emergent non-serious adverse events \[TEAEs\]).