4D-150 IVT (3E10 vg/eye)
BiologicalIf randomized to the 4D-150 treatment arm, 4D-150 will be administered at the assigned dose level as a single dose IVT injection on Day 1
NCT Number: NCT07064759
A Phase 3, Randomized, Double-Masked, Active-Controlled Trial in Adults with Macular Neovascularization Secondary to Age-Related Macular Degeneration
Interested in participating?
Request Info50 year and older
All sexes
Interventional
Phase 3
Grupo Láser Visión, Rosario, Santa Fe Province, Argentina
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Ocular Conditions:
Ocular Treatments/Interventions:
Systemic Conditions and Considerations:
If randomized to the 4D-150 treatment arm, 4D-150 will be administered at the assigned dose level as a single dose IVT injection on Day 1
Eylea (aflibercept) will be administered at applicable visits
Time frame: 52 Weeks
Time frame: 104 Weeks
Time frame: 104 Weeks
Time frame: 104 Weeks
Time frame: 104 Weeks
Time frame: 104 Weeks
Contact information is provided by the study sponsor or research team.
4D Molecular Therapeutics
Industry
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
Acronym: 4FRONT-2
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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