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NCT00913744 · ClinicalTrials.gov registry record · Phase 2

Safety and Efficacy Study of Intravitreal Ocriplasmin in Subjects With AMD With Focal Vitreomacular Adhesion

A Phase 2 study, sponsored by ThromboGenics.

Completed
Registry status
Phase 2
Development phase
100
Enrollment target

NCT00913744: Completed Phase 2 study, sponsored by ThromboGenics.

NCT00913744 is a Phase 2 study that has completed, run by ThromboGenics. The registered enrollment target is 100 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (25% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00913744, a Phase 2 study, has completed, sponsored by ThromboGenics.

COMPLETED
Registry status
Phase 2
Development phase
100 participants
Enrollment target

Study Summary

This study will evaluate the safety and efficacy of Ocriplasmin intravitreal injection, in subjects diagnosed with exudative AMD with focal vitreomacular adhesion. Ultimately, it is believed that intravitreal ocriplasmin may offer physicians a safe agent for pharmacologic vitreolysis and nonsurgical resolution of focal vitreomacular adhesion in AMD subjects where this adhesion may be causally associated with worse prognosis).

Primary Outcome

The VMA release was determined by masked Central Reading Center Optical Coherence Tomography (OCT) evaluation

Interventions

  • DRUG Sham injection
  • DRUG Ocriplasmin

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2010-01
Est. Completion 2013-04
Phase Phase 2
ThromboGenics

12 total trials

What the finished NCT00913744 record still lists

NCT00913744 is an interventional study that assigns participants to a tested intervention. The registered 100 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 (25% lower).

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

NCT00913744 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00913744 about?

NCT00913744 is a clinical study titled "Safety and Efficacy Study of Intravitreal Ocriplasmin in Subjects With AMD With Focal Vitreomacular Adhesion". This study will evaluate the safety and efficacy of Ocriplasmin intravitreal injection, in subjects diagnosed with exudative AMD with focal vitreomacular adhesion. Ultimately, it is believed that intravitreal ocriplasmin may offer physicians a safe agent for pharmacologic vitreolysis and nonsurgical...

What is the current status of trial NCT00913744?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 100 participants. The study started on 2010-01. Estimated completion is 2013-04.

What interventions are being tested in trial NCT00913744?

The interventions under investigation include: Sham injection (DRUG), Ocriplasmin (DRUG).

Who is sponsoring clinical trial NCT00913744?

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

How this trial's enrollment target compares

Where NCT00913744's enrollment target sits among peer trials

100 672nd of 2000 higher than 1,263 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 NCT00913744, the US trial registry maintained by the National Library of Medicine. NCT00913744 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.