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NCT00211432 · ClinicalTrials.gov registry record · Phase 2

Treatment of Pseudovitellium Detachment With Open-Label Anecortave Acetate Sterile Suspension (15 mg)

A Phase 2 study, sponsored by Manhattan Eye, Ear & Throat Hospital.

Completed
Registry status
Phase 2
Development phase
4
Enrollment target

NCT00211432: Completed Phase 2 study, sponsored by Manhattan Eye, Ear & Throat Hospital.

NCT00211432 is a Phase 2 study that has completed, run by Manhattan Eye, Ear & Throat Hospital. The registered enrollment target is 4 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00211432, a Phase 2 study, has completed, sponsored by Manhattan Eye, Ear & Throat Hospital.

COMPLETED
Registry status
Phase 2
Development phase
4 participants
Enrollment target

Study Summary

The purpose of this study is to provide compassionate use of anecortave acetate sterile suspension of 15 mg for a series of five patients as a means to control pseudovitelliform detachment.

Interventions

  • DRUG Anecortave Acetate Sterile Suspension (15 mg)

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2008-04
Est. Completion 2010-04
Phase Phase 2

What the finished NCT00211432 record still lists

NCT00211432 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 4 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which Anecortave Acetate Sterile Suspension (15 mg) is the first listed.

NCT00211432 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00211432 about?

NCT00211432 is a clinical study titled "Treatment of Pseudovitellium Detachment With Open-Label Anecortave Acetate Sterile Suspension (15 mg)". The purpose of this study is to provide compassionate use of anecortave acetate sterile suspension of 15 mg for a series of five patients as a means to control pseudovitelliform detachment.

What is the current status of trial NCT00211432?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 4 participants. The study started on 2008-04. Estimated completion is 2010-04.

What interventions are being tested in trial NCT00211432?

The interventions under investigation include: Anecortave Acetate Sterile Suspension (15 mg) (DRUG).

Who is sponsoring clinical trial NCT00211432?

This trial is sponsored by Manhattan Eye, Ear & Throat Hospital, which has 14 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00211432's enrollment target sits among peer trials

4 2001st of 2000 the lowest 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 NCT00211432, the US trial registry maintained by the National Library of Medicine. NCT00211432 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.