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NCT00271167 · ClinicalTrials.gov registry record · Phase 2

A Trial of INO-1001 in Patients Undergoing Heart Surgery That Involves Heart-lung Bypass

A Phase 2 study, sponsored by Inotek Pharmaceuticals Corporation.

Terminated
Registry status
Phase 2
Development phase
162
Enrollment target

NCT00271167: Clinical Trial Phase 2 study, sponsored by Inotek Pharmaceuticals Corporation.

NCT00271167 is a Phase 2 study that was terminated before completion, run by Inotek Pharmaceuticals Corporation. The registered enrollment target is 162 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (22% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00271167, a Phase 2 study, was terminated before completion, sponsored by Inotek Pharmaceuticals Corporation.

TERMINATED
Registry status
Phase 2
Development phase
162 participants
Enrollment target

Study Summary

The purpose of this study is to assess the safety of INO-1001, an intravenous PARP (poly-\[ADP ribose\] polymerase) inhibitor, in patients undergoing heart surgery. The study also measures whether INO-1001 reduces the side effects caused by heart-lung bypass machines.

Interventions

  • DRUG INO-1001

Trial Details

FieldValue
Enrollment Target 162 participants
Start Date 2005-10
Est. Completion 2006-06
Phase Phase 2

Why NCT00271167 stopped before completion

NCT00271167 is an interventional study that assigns participants to a tested intervention. The registered 162 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (22% higher).

The record links to 0 conditions, and to 1 intervention - of which INO-1001 is the first listed.

NCT00271167 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00271167 about?

NCT00271167 is a clinical study titled "A Trial of INO-1001 in Patients Undergoing Heart Surgery That Involves Heart-lung Bypass". The purpose of this study is to assess the safety of INO-1001, an intravenous PARP (poly-\[ADP ribose\] polymerase) inhibitor, in patients undergoing heart surgery. The study also measures whether INO-1001 reduces the side effects caused by heart-lung bypass machines.

What is the current status of trial NCT00271167?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 162 participants. The study started on 2005-10. Estimated completion is 2006-06.

What interventions are being tested in trial NCT00271167?

The interventions under investigation include: INO-1001 (DRUG).

Who is sponsoring clinical trial NCT00271167?

This trial is sponsored by Inotek Pharmaceuticals Corporation, which has 7 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00271167's enrollment target sits among peer trials

162 418th of 2000 higher than 1,579 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 NCT00271167, the US trial registry maintained by the National Library of Medicine. NCT00271167 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.