Hemoglobin Based Oxygen Therapeutics in Elective Percutaneous Coronary Revascularization

Acute Coronary Syndrome Clinical Trial

Official title:

Phase II, Open-Label Study in the Catheterization Laboratory Setting to Challenge the Concept That HBOC-201 Administration Might Improve Myocardial 'Oxygenation' and Myocardial Function at the Moment of (Brief) Coronary Occlusion

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00479895
• Other study ID #: COR-0002
• Status: Completed
• Phase: Phase 2
• First received: May 25, 2007
• Last updated: May 29, 2008
• Start date: April 2007
• Est. completion date: April 2008

Study information

• Verified date: May 2008
• Source: Biopure Corporation
• Contact: n/a
• Is FDA regulated: No
• Health authority: Netherlands: Medical Ethics Review Committee of the Erasmus Medical Center, Rotterdam
• Study type: Interventional

Clinical Trial Summary

The test compound and subject of this clinical trial is the haemoglobin-based oxygen carrier, HBOC-201 (Hemopure). HBOC-201, initially developed as an alternative to red blood cells for surgical patients, has the ability to restore tissue oxygenation in persistently ischemic tissue. The development of this new class of compounds, referred to as oxygen therapeutics, provides an opportunity to test the safety and efficacy of a new approach to management of myocardial ischemia.

Description:

Because of their ability to perfuse and deliver oxygen, hemoglobin-based oxygen carriers (HBOC) may be considered in the treatment of several ischemic conditions, such as acute coronary syndromes (ACS). Elective percutaneous intervention (PCI) induces transient myocardial ischemia due to reduction of coronary flow during balloon inflation in the coronary artery, thus simulating in a control setting, the occurrence of an ACS.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 5
• Est. completion date: April 2008
• Est. primary completion date: March 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Signed informed consent before initiation of any study-related procedure and agreement to comply with all protocol-specific procedures

• Stable angina pectoris (CCS Class 1, 2, 3, 4) or unstable angina (Braundwald class 1-3, B) or documented silent ischemia

• Baseline ECG with stable sinus rhythm and no signs of ischemia and with no Q waves, bundle branch block or IV conduction disturbances.

• Normal left ventricular wall motion on left ventricular angiogram or on echocardiogram with preserved systolic global LV function

• Non-occlusive stenosis, located in the proximal segments of the left anterior descending artery (LAD) (segments 6 and/or 7) and/or circumflex artery (CFX) (segments 11 and/or 12) or right coronary artery (RCA) (segments 1, 2 and/or 3) for which there is clinical indication to percutaneous treatment with coronary stenting

• Successful PCI with stenting on the target vessel

• Older than 18 years and younger than 80 years of age

Exclusion Criteria:

• Active ischemia at the initiation of the study procedure

• Non-ST segment elevation myocardial infarction

• History or ECG evidence of prior MI in the territory supplied by the vessel undergoing PCI, IV conduction defects/baseline ST-segment abnormalities on the surface ECG

• Moderate to severe aortic or mitral valve disease

• Evidence of LV hypertrophy on the echocardiogram IVS > 13 and/or PW > 13mm

• Angiographically visible collateral vessels to the target vessel

• Hypertension not adequately controlled by anti-hypertensive therapy at the time of study entry (> 140/100mmHg)

• Uncompensated congestive heart failure or signs of pulmonary edema

• Significant hemodynamic compromise and/or cardiogenic shock requiring inotropic or pressor support

• Contraindications to standard drugs for coronary intervention and coronary heart disease: aspirin, heparin, low molecular weight heparin, clopidogrel, contrast dye

• Confirmed pregnancy

• Systemic mastocytosis

• Hypoxemia (need for mechanical ventilation

• Known history of COPD with FEV 1s < 1.0 liter

• Renal impairment: creatinine > 1.6 mg/dl

• Participation in another trial with an investigational drug or device including follow-up period, within the last 30 days before enrollment

Additional exclusion criteria at the end of PCI (before randomization)

• Coronary TIMI flow in the treated artery is less than 3

• Serious arrhythmias during/following the PCI was noted

• Coronary spasm following PCI

• Any deterioration in the subject's "risk" status between informed consent and randomization

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Acute Coronary Syndrome
• Coronary Occlusion

Intervention

Drug:
• Hemoglobin Based Oxygen Carrier-201 (HBOC-201, Hemopure)
Pre-oxygenated HBOC-201

Locations

Country	Name	City	State
Netherlands	Thoraxcentre - Erasmus MC	Rotterdam

Sponsors (1)

Lead Sponsor	Collaborator
Biopure Corporation

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To study the change in left ventricular relaxation indices and pressure-half time and the change in the sum of ST segment deviations compared to baseline.		Duration of the study	No
Secondary	LV hemodynamics; change of ST segment; QCA analysis before and after the no-infusion control occlusion and HBOC-201 infusion/occlusion; safety endpoints		Duration of the study