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

Inotek Pharmaceuticals

Status and phase

Terminated

Phase 2

Conditions

Postoperative Complications

Heart Diseases

Treatments

Drug: INO-1001

Study type

Interventional

Funder types

Industry

Identifiers

NCT00271167

IPC-05-2004

Details and patient eligibility

About

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.

Full description

Heart-lung bypass during heart surgery sometimes leads to side effects or complications after surgery.

Studies have shown that PARP inhibitors protect cells from damage due to lack of oxygen. Heart-lung bypass during heart surgery can result in cells being deprived of oxygen. INO-1001 may be able to protect these cells and reduce complications following surgery.

A total of 162 patients will be randomly assigned to either INO-1001 or placebo (sugar water). Treatment will begin on the day of heart surgery and continue for 36 hours. A total of 4 doses of INO-1001 will be given. Patients will be followed up until 30 days after surgery.

The following information will be collected: symptoms, vital signs, physical examination, blood and urine tests, electrocardiograms, and other information from medical charts.

The information provided in this listing is disclosed solely to comply with regulatory requirements. The drug INO-1001 has not yet been approved for marketing and is only available to patients who participate in a clinical trial and are chosen for the treatment group.

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients scheduled to undergo cardiopulmonary bypass for coronary revascularization and/or valve surgery
Males and non-pregnant, non-lactating females

Exclusion criteria

Subjects will be required to undergo a full medical review in order to exclude serious medical or psychological illness prior to inclusion
History of a hypersensitivity reaction to more than three drugs or to mannitol
Participation in any other investigational study within 30 days of the screening phase
Known alcohol or drug abuse within the last year
Treatment with certain restricted medications within a specified time prior to participation in the study