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NCT00271765 · ClinicalTrials.gov registry record · Phase 2

A Study of INO-1001, an Intravenous PARP (Poly [ADP Ribose] Polymerase) Inhibitor in Acute Heart Attack Patients Undergoing Primary Percutaneous Coronary Intervention

A Phase 2 study of Acute Myocardial Infarction, sponsored by Inotek Pharmaceuticals Corporation.

Completed
Registry status
Phase 2
Development phase
40
Enrollment target
16
Study locations

NCT00271765 is a Phase 2 study of Acute Myocardial Infarction that has completed, run by Inotek Pharmaceuticals Corporation. The registered enrollment target is 40 participants, below the 1,880-participant average among 19 other Acute Myocardial Infarction trials with a reported enrollment target (98% lower). The trial reports 16 study locations across 11 states.

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The verdict

NCT00271765, a Phase 2 study of Acute Myocardial Infarction, has completed, sponsored by Inotek Pharmaceuticals Corporation.

COMPLETED
Registry status
Phase 2
Development phase
40 participants
Enrollment target
16
Study locations

Study Summary

The primary purpose of this study is to assess the safety of INO-1001 in subjects who have experienced a heart attack and are to be treated with coronary angioplasty.

Interventions

  • DRUG INO-1001

Study Locations (16)

Other

  • Rambam Medical Center - Haifa
  • Meir Medical Center - Kfar Saba
  • Hasharon Medical Center - Petah Tikva
  • Rabin Medical Center - Petah Tikva
  • - Rehovot
  • Assaf Harofe Medical Centre - Ẕerifin

Florida

  • Holy Cross Hospital - Fort Lauderdale

Indiana

  • Porter Hospital - Valparaiso

Minnesota

  • St. Paul Heart Clinic - Saint Paul

New Jersey

  • - Newark

Ohio

  • Toledo Hospital - Toledo

Pennsylvania

  • Hospital of the University of Pennsylvania - Philadelphia

South Dakota

  • Black Hills Cardiovascular Research - Rapid City

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2004-01
Est. Completion 2006-06
Phase Phase 2

What the Registry Record Tells You About NCT00271765

The ClinicalTrials.gov registry entry for NCT00271765 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,880-participant average among 19 other Acute Myocardial Infarction trials with a reported enrollment target (98% lower). The listed sponsor is Inotek Pharmaceuticals Corporation, which has 7 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Acute Myocardial Infarction appearing as the primary indexed condition, and to 1 intervention - of which INO-1001 is the first listed.

NCT00271765 reports 16 study locations spanning 11 distinct geographic areas - top geographies include Other, Florida, Indiana.

Frequently Asked Questions

What is clinical trial NCT00271765 about?

NCT00271765 is a clinical study titled "A Study of INO-1001, an Intravenous PARP (Poly [ADP Ribose] Polymerase) Inhibitor in Acute Heart Attack Patients Undergoing Primary Percutaneous Coronary Intervention". The primary purpose of this study is to assess the safety of INO-1001 in subjects who have experienced a heart attack and are to be treated with coronary angioplasty.

What is the current status of trial NCT00271765?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2004-01. Estimated completion is 2006-06.

What conditions does trial NCT00271765 study?

This clinical trial studies the following conditions: Acute Myocardial Infarction.

What interventions are being tested in trial NCT00271765?

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

Who is sponsoring clinical trial NCT00271765?

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

Where is trial NCT00271765 being conducted?

This trial has 16 study locations across Florida, Indiana, Minnesota, New Jersey, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.