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NCT05383209 · ClinicalTrials.gov registry record · Phase 2

Study of EYP-1901 in Patients With Nonproliferative Diabetic Retinopathy (NPDR)

A Phase 2 study, sponsored by EyePoint Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
77
Enrollment target

NCT05383209: Completed Phase 2 study, sponsored by EyePoint Pharmaceuticals.

NCT05383209 is a Phase 2 study that has completed, run by EyePoint Pharmaceuticals. The registered enrollment target is 77 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (42% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05383209, a Phase 2 study, has completed, sponsored by EyePoint Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
77 participants
Enrollment target

Study Summary

A prospective, randomized, double-masked study that evaluated the ocular efficacy and safety of two doses of the EYP-1901 intravitreal (IVT) insert compared to sham.

Primary Outcome

The DRSS used to describe overall retinopathy severity as well as the change in severity over time in the study eye. Severity ranges from level 10 (diabetic retinopathy absent) to level 85 (advanced proliferative diabetic retinopathy (PDR): posterior fundus obscured, or center of macula detached). Here, DRSS describes severity level 47 (moderately severe NPDR) and level 53 (severe NPDR) at Week 36 from baseline.

Interventions

  • DRUG EYP-1901
  • OTHER Sham IVT

Trial Details

FieldValue
Enrollment Target 77 participants
Start Date 2022-09-28
Est. Completion 2024-05-06
Phase Phase 2
EyePoint Pharmaceuticals

16 total trials

What the finished NCT05383209 record still lists

NCT05383209 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 77 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (42% lower).

The record links to 0 conditions, and to 2 interventions - of which EYP-1901 is the first listed.

NCT05383209 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05383209 about?

NCT05383209 is a clinical study titled "Study of EYP-1901 in Patients With Nonproliferative Diabetic Retinopathy (NPDR)". A prospective, randomized, double-masked study that evaluated the ocular efficacy and safety of two doses of the EYP-1901 intravitreal (IVT) insert compared to sham.

What is the current status of trial NCT05383209?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 77 participants. The study started on 2022-09-28. Estimated completion is 2024-05-06.

What interventions are being tested in trial NCT05383209?

The interventions under investigation include: EYP-1901 (DRUG), Sham IVT (OTHER).

Who is sponsoring clinical trial NCT05383209?

This trial is sponsored by EyePoint Pharmaceuticals, which has 16 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05383209's enrollment target sits among peer trials

77 891st of 2000 higher than 1,108 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05383209, the US trial registry maintained by the National Library of Medicine. NCT05383209 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.