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Clinical Trials in the EU / 2025-521349-25-00
Terminated Phase III

A Phase 3, Randomized, Double-Masked, Active-Controlled Trial of a Single Intravitreal Injection of 4D-150 in Adults with Macular Neovascularization Secondary to Age-Related Macular Degeneration (4FRONT-2)

2025-521349-25-00 · tracked via the Priya Life Science EU tracker
Sponsor
4d Molecular Therapeutics Inc.
Sponsor type
Pharmaceutical company
Therapeutic area
Eye Diseases
Decision date
21/11/2025
Enrollment target
298
Sites
Germany, Italy, Hungary, Bulgaria, Lithuania, France, Spain, Latvia, Portugal

Condition studied

Macular neovascularization secondary to age-related macular degeneration (nAMD)

Investigational medicinal product(s)

Eylea 40 mg/mL solution for injection in pre-filled syringe4D-150Eylea 40 mg/mL solution for injection in pre-filled syringeEylea 40 mg/mL solution for injection in pre-filled syringeDIFLUPREDNATEEylea 40 mg/mL solution for injection in pre-filled syringe

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

Primary endpoint

Mean change from baseline in BCVA ETDRS letter score at Week 52

Endpoint detail

Mean annualized number of aflibercept injections after Week 4 through Weeks 52 and 104, Incidence and timing of aflibercept injections after Week 4 through Weeks 52 and 104, Proportion of subjects not requiring aflibercept injections after Week 4 through Weeks 52 and 104 in the 4D-150 arm, Time to first aflibercept injection after Week 4 in the 4D-150 arm, Mean change from baseline in CST over time through Weeks 52 and 104, Mean change from baseline in BCVA ETDRS letter score over time through Weeks 52 and 104

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-521349-25-00 on CTIS ↗ ← All trials in the EU