drugset / Trial / NCT07557121

Safety and Efficacy of AIV007 Periocular Injection in Patients With Neovascular Age-Related Macular Degeneration

NCT07557121

Phase 2 Not yet recruiting 35 enrolled AiViva BioPharma, Inc. ClinDatrix, Inc. · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

The goal of this study is to evaluate whether AIV007 provides benefits to patients with neovascular age-related macular degeneration in improving vision and that it has an acceptable safety profile. Participants will receive either a periocular injection of AIV007 or intravitreal injection of Eylea (control arm) to the study eye and return to the clinic monthly for safety and efficacy observations and/or continued treatment. Participants may receive additional treatment(s) if they meet specified criteria.

Timeline

Start
2026-07-01
Primary completion
2027-06-30
Completion
2027-08-23

Drugs

EvaluationDrugModalityDoseRoute
Subject AIV007 Unknown 6 mg Other
Subject AIV007 Unknown 8 mg Other
Comparator Aflibercept Protein / enzyme biologic 2 mg Intravitreal