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Active Not RecruitingNCT06683742

A 2-year Study of EYP-1901 in Subjects With Wet Age Related Macular Degeneration (wAMD) (LUCIA) Primary Efficacy Will be Determined at Week 56

A 2-year Phase 3, Multicenter, Prospective, Randomized, Double-Masked, Parallel-Group Study of EYP-1901, a Tyrosine Kinase Inhibitor (TKI), Compared to Aflibercept in Subjects With Wet AMD

Status
Active Not Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
400 (estimated)
Sponsor
EyePoint Pharmaceuticals, Inc. · Industry
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

This is a phase 3 randomized, double -masked study comparing the efficacy of EYP-1901 against Aflibercept.

Conditions

Interventions

TypeNameDescription
DRUGEYP-1901Intravitreal Injection
DRUGAflibercept (2.0 mg)Intravitreal Injection

Timeline

Start date
2024-11-27
Primary completion
2026-10-01
Completion
2027-10-01
First posted
2024-11-12
Last updated
2026-04-02

Locations

129 sites across 10 countries: United States, Brazil, Czechia, Germany, Hungary, India, Israel, Poland, Slovakia, United Kingdom

Regulatory

Source: ClinicalTrials.gov record NCT06683742. Inclusion in this directory is not an endorsement.

A 2-year Study of EYP-1901 in Subjects With Wet Age Related Macular Degeneration (wAMD) (LUCIA) Primary Efficacy Will be (NCT06683742) · Clinical Trials Directory