Viewing Study NCT00271167


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Study NCT ID: NCT00271167
Status: TERMINATED
Last Update Posted: 2015-03-25
First Post: 2005-12-29
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: A Trial of INO-1001 in Patients Undergoing Heart Surgery That Involves Heart-lung Bypass
Sponsor:
Organization:

Raw JSON

{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D006331', 'term': 'Heart Diseases'}, {'id': 'D011183', 'term': 'Postoperative Complications'}], 'ancestors': [{'id': 'D002318', 'term': 'Cardiovascular Diseases'}, {'id': 'D010335', 'term': 'Pathologic Processes'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'C491685', 'term': 'INO 1001'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'DOUBLE'}, 'primaryPurpose': 'PREVENTION', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'count': 162}}, 'statusModule': {'whyStopped': 'It was determined that the study was not appropriate for demonstrating therapeutic benefit in the cardiopulmonary bypass patient population.', 'overallStatus': 'TERMINATED', 'startDateStruct': {'date': '2005-10'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2015-03', 'completionDateStruct': {'date': '2006-06', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2015-03-23', 'studyFirstSubmitDate': '2005-12-29', 'studyFirstSubmitQcDate': '2005-12-29', 'lastUpdatePostDateStruct': {'date': '2015-03-25', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2005-12-30', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Reduction in serious post-operative complications occurring in the first thirty days after surgery.'}]}, 'conditionsModule': {'keywords': ['Cardiac surgery', 'PARP inhibitor', 'PARP inhibition', 'Bypass surgery', 'CPB surgery', 'Cardiopulmonary bypass', 'Coronary revascularization', 'Cardiac valve replacement'], 'conditions': ['Heart Diseases', 'Postoperative Complications']}, 'referencesModule': {'references': [{'pmid': '12892811', 'type': 'BACKGROUND', 'citation': 'Khan TA, Ruel M, Bianchi C, Voisine P, Komjati K, Szabo C, Sellke FW. Poly(ADP-ribose) polymerase inhibition improves postischemic myocardial function after cardioplegia-cardiopulmonary bypass. J Am Coll Surg. 2003 Aug;197(2):270-7. doi: 10.1016/S1072-7515(03)00538-6.'}, {'pmid': '12223530', 'type': 'BACKGROUND', 'citation': 'Virag L, Szabo C. The therapeutic potential of poly(ADP-ribose) polymerase inhibitors. Pharmacol Rev. 2002 Sep;54(3):375-429. doi: 10.1124/pr.54.3.375.'}, {'pmid': '16026326', 'type': 'BACKGROUND', 'citation': 'Szabo C. Pharmacological inhibition of poly(ADP-ribose) polymerase in cardiovascular disorders: future directions. Curr Vasc Pharmacol. 2005 Jul;3(3):301-3. doi: 10.2174/1570161054368553.'}]}, 'descriptionModule': {'briefSummary': '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.', 'detailedDescription': 'Heart-lung bypass during heart surgery sometimes leads to side effects or complications after surgery.\n\nStudies 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.\n\nA 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.\n\nThe following information will be collected: symptoms, vital signs, physical examination, blood and urine tests, electrocardiograms, and other information from medical charts.\n\nThe 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.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '90 Years', 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Patients scheduled to undergo cardiopulmonary bypass for coronary revascularization and/or valve surgery\n* Males and non-pregnant, non-lactating females\n\nExclusion Criteria:\n\n* Subjects will be required to undergo a full medical review in order to exclude serious medical or psychological illness prior to inclusion\n* History of a hypersensitivity reaction to more than three drugs or to mannitol\n* Participation in any other investigational study within 30 days of the screening phase\n* Known alcohol or drug abuse within the last year\n* Treatment with certain restricted medications within a specified time prior to participation in the study'}, 'identificationModule': {'nctId': 'NCT00271167', 'briefTitle': 'A Trial of INO-1001 in Patients Undergoing Heart Surgery That Involves Heart-lung Bypass', 'organization': {'class': 'INDUSTRY', 'fullName': 'Inotek Pharmaceuticals Corporation'}, 'officialTitle': 'A Phase II Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Evaluate Tolerability, Safety, Pharmacokinetics and Efficacy of Intravenous INO-1001 in High Risk Subjects Undergoing Cardiopulmonary Bypass for Coronary Revascularization and/or Valve Surgery.', 'orgStudyIdInfo': {'id': 'IPC-05-2004'}}, 'armsInterventionsModule': {'interventions': [{'name': 'INO-1001', 'type': 'DRUG'}]}, 'contactsLocationsModule': {'locations': [{'zip': '02215', 'city': 'Boston', 'state': 'Massachusetts', 'country': 'United States', 'facility': 'Beth Israel Deaconess Medical Center', 'geoPoint': {'lat': 42.35843, 'lon': -71.05977}}, {'zip': '73152', 'city': 'Oklahoma City', 'state': 'Oklahoma', 'country': 'United States', 'facility': 'University of Oklahoma', 'geoPoint': {'lat': 35.46756, 'lon': -97.51643}}, {'zip': '19104', 'city': 'Philadelphia', 'state': 'Pennsylvania', 'country': 'United States', 'facility': 'University of Pennsylvania', 'geoPoint': {'lat': 39.95238, 'lon': -75.16362}}, {'city': 'Rapid City', 'state': 'South Dakota', 'country': 'United States', 'facility': 'Rapid City Regional Hospital', 'geoPoint': {'lat': 44.08054, 'lon': -103.23101}}, {'zip': '77030', 'city': 'Houston', 'state': 'Texas', 'country': 'United States', 'facility': 'Methodist Hospital', 'geoPoint': {'lat': 29.76328, 'lon': -95.36327}}, {'city': 'Sydney', 'state': 'New South Wales', 'country': 'Australia', 'geoPoint': {'lat': -33.86785, 'lon': 151.20732}}, {'city': 'Adelaide', 'state': 'South Australia', 'country': 'Australia', 'facility': 'Ashford Cardiac Clinic / Adelaide Cardiac', 'geoPoint': {'lat': -34.92866, 'lon': 138.59863}}, {'zip': '3065', 'city': 'Melbourne', 'state': 'Victoria', 'country': 'Australia', 'facility': "St. Vincent's Hospital", 'geoPoint': {'lat': -37.814, 'lon': 144.96332}}, {'zip': '6000', 'city': 'Perth', 'state': 'Western Australia', 'country': 'Australia', 'facility': 'Royal Perth Hospital', 'geoPoint': {'lat': -31.95224, 'lon': 115.8614}}, {'city': 'Hyderabad', 'country': 'India', 'facility': 'Care Hospital', 'geoPoint': {'lat': 17.38405, 'lon': 78.45636}}, {'zip': '110029', 'city': 'New Delhi', 'country': 'India', 'facility': 'Escorts Heart Institute and Research Centre', 'geoPoint': {'lat': 28.62137, 'lon': 77.2148}}, {'zip': '58100', 'city': 'Holon', 'country': 'Israel', 'facility': 'Wolfson Medical Centre', 'geoPoint': {'lat': 32.01034, 'lon': 34.77918}}, {'city': 'Jerusalem', 'country': 'Israel', 'geoPoint': {'lat': 31.76904, 'lon': 35.21633}}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Inotek Pharmaceuticals Corporation', 'class': 'INDUSTRY'}}}}