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NCT00770770 · ClinicalTrials.gov registry record · Phase 2

Fluocinolone Acetonide Intravitreal Inserts for Vein Occlusion in Retina

A Phase 2 study, sponsored by Alimera Sciences.

Terminated
Registry status
Phase 2
Development phase
20
Enrollment target

NCT00770770: Clinical Trial Phase 2 study, sponsored by Alimera Sciences.

NCT00770770 is a Phase 2 study that was terminated before completion, run by Alimera Sciences. The registered enrollment target is 20 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00770770, a Phase 2 study, was terminated before completion, sponsored by Alimera Sciences.

TERMINATED
Registry status
Phase 2
Development phase
20 participants
Enrollment target

Study Summary

This study will assess the safety and efficacy of FA Intravitreal Inserts in subjects with macular edema secondary to RVO.

Primary Outcome

To compare the 3 month best corrected visual acuity to baseline in subjects diagnosed with macular edema secondary to retinal vein occlusion. BCVA will be measured according to the standard procedure developed for ETDRS at 4 meters or 3 meters if the electronic (E)-ETDRS system is employed.

Interventions

  • DRUG Fluocinolone Acetonide

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2009-05
Phase Phase 2
Alimera Sciences

8 total trials

Why NCT00770770 stopped before completion

NCT00770770 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower).

The record links to 0 conditions, and to 1 intervention - of which Fluocinolone Acetonide is the first listed.

NCT00770770 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00770770 about?

NCT00770770 is a clinical study titled "Fluocinolone Acetonide Intravitreal Inserts for Vein Occlusion in Retina". This study will assess the safety and efficacy of FA Intravitreal Inserts in subjects with macular edema secondary to RVO.

What is the current status of trial NCT00770770?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2009-05.

What interventions are being tested in trial NCT00770770?

The interventions under investigation include: Fluocinolone Acetonide (DRUG).

Who is sponsoring clinical trial NCT00770770?

This trial is sponsored by Alimera Sciences, which has 8 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00770770's enrollment target sits among peer trials

20 1805th of 2000 higher than 107 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 NCT00770770, the US trial registry maintained by the National Library of Medicine. NCT00770770 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.