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4D-150 in Patients With Diabetic Macular Edema

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NCT05930561 · readout in 924 d

Sponsored by 4D Molecular Therapeutics (industry) · FDMT — their whole pipeline →.

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · Double · Treatment
Enrollment
72estimated
Sites
6
Countries
Puerto Rico, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-08-09actualWhen the study began enrolling
Primary completion2029-02-28estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-02-28estimatedThe whole study's end, after follow-up
First posted2023-07-05actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-09-22actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Diabetic Macular Edema
  • Diabetic Retinopathy

Interventions

  • Biological: 4D-150 IVT
  • Biological: Aflibercept IVT — also filed as Eylea

Primary outcomes

what the primary-completion date above is the date OF
Incidence and severity of TEAEs and SAEs, including clinically significant changes in safety parameters (Part 1)
measured 60 months
Annualized number of aflibercept injections in the study eye (Part 2)
measured 52 weeks

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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