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NCT03180255 · ClinicalTrials.gov registry record · Phase 2

Iontophoretic Delivery of EGP-437 in Patients Who Have Undergone Cataract Surgery

A Phase 2 study, sponsored by Eyegate Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
101
Enrollment target

NCT03180255: Completed Phase 2 study, sponsored by Eyegate Pharmaceuticals.

NCT03180255 is a Phase 2 study that has completed, run by Eyegate Pharmaceuticals. The registered enrollment target is 101 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (24% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03180255, a Phase 2 study, has completed, sponsored by Eyegate Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
101 participants
Enrollment target

Study Summary

Phase 2b trial evaluating the safety and efficacy of EGP-437, versus placebo using the EyeGate® II Drug Delivery System (EGDS) in patients having undergone cataract surgery with implantation of a monofocal posterior chamber intraocular lens (IOL).

Primary Outcome

The proportion of subjects with an AC cell count of zero on Day 7

Interventions

  • OTHER Placebo
  • COMBINATION_PRODUCT Dexamethasone phosphate

Trial Details

FieldValue
Enrollment Target 101 participants
Start Date 2017-07-26
Est. Completion 2017-11-27
Phase Phase 2
Eyegate Pharmaceuticals

12 total trials

What the finished NCT03180255 record still lists

NCT03180255 is an interventional study that assigns participants to a tested intervention. The registered 101 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (24% lower).

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

NCT03180255 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03180255 about?

NCT03180255 is a clinical study titled "Iontophoretic Delivery of EGP-437 in Patients Who Have Undergone Cataract Surgery". Phase 2b trial evaluating the safety and efficacy of EGP-437, versus placebo using the EyeGate® II Drug Delivery System (EGDS) in patients having undergone cataract surgery with implantation of a monofocal posterior chamber intraocular lens (IOL).

What is the current status of trial NCT03180255?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 101 participants. The study started on 2017-07-26. Estimated completion is 2017-11-27.

What interventions are being tested in trial NCT03180255?

The interventions under investigation include: Placebo (OTHER), Dexamethasone phosphate (COMBINATION_PRODUCT).

Who is sponsoring clinical trial NCT03180255?

This trial is sponsored by Eyegate Pharmaceuticals, which has 12 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03180255's enrollment target sits among peer trials

101 672nd of 2000 higher than 1,329 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 NCT03180255, the US trial registry maintained by the National Library of Medicine. NCT03180255 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.