Skip to main content
Clinical Trials/NCT00317512
NCT00317512
Completed
Phase 2

A Multi-Center,Randomized,Double-Blind,Placebo-Controlled,Dose Finding Pilot Study, to Evaluate Safety/Feasibility of HBOC-201 in Elective Percutaneous Coronary Revascularization of Subjects With Acute Coronary Syndromes

Biopure Corporation6 sites in 3 countries45 target enrollmentDecember 2003

Overview

Phase
Phase 2
Intervention
Percutaneous Coronary Revascularization
Conditions
Angina Pectoris
Sponsor
Biopure Corporation
Enrollment
45
Locations
6
Primary Endpoint
Safety
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

The purpose of this study is to assess the safety and feasibility of a novel oxygen carrying solution, HBOC-201, in the setting of PCI for Acute Coronary Syndromes from randomization til hospital discharge.

Detailed Description

Acute coronary syndromes are due to an acute or subacute primary reduction of myocardial oxygen supply provoked by disruption of an atherosclerotic plaque associated with inflammation, thrombosis, vasoconstriction and microembolization. Occlusive thrombosis superimposed on a ruptured atheroma in an epicardial coronary artery is firmly established as the immediate cause of an acute ST-segment Elevation Myocardial Infarction (STEMI). Rapid restoration of blood flow (oxygen supply) to jeopardized myocardium limits necrosis and reduces mortality. This can be accomplished medically with a thrombolytic agent, or mechanically, with so-called primary balloon angioplasty or stenting. Primary percutaneous coronary intervention (PCI) has become the preferred therapy for STEMI in most developed countries. HBOC-201 is a solution belonging to a new class of biologic oxygen therapeutics, hemoglobin based oxygen carriers. HBOC-201 is a crosslinked and glutaraldehyde-polymerized hemoglobin (Hb) extracted from isolated bovine red blood cells. On a gram-for-gram basis, HBOC-201 was calculated to be approximately three times more potent than stored fresh red blood cell hemoglobin at restoring baseline tissue oxygenation following severe acute anemia. Evaluation of this Hemoglobin Based Oxygen Carrier has been undertaken in 57 preclinical studies and 21 human clinical trials. The compound is under review by the US FDA and has been approved in the Republic of South Africa. However, HBOC-201 has not yet been evaluated in the setting of this disease (narrowing of a coronary artery). Biopure will be studying the safety and feasibility of HBOC-201 in patients with typical symptoms of Unstable Angina or Non ST-segment Elevation Myocardial Infarction eligible to undergo invasive revascularization through a PCI procedure.

Registry
clinicaltrials.gov
Start Date
December 2003
End Date
July 2007
Last Updated
17 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Sponsor
Biopure Corporation

Eligibility Criteria

Inclusion Criteria

  • Written informed consent provided before initiation of any study-related procedure, and before any pre-procedural sedation, and agreement to comply with all protocol-specified procedures
  • Acute Coronary Syndrome (Stable and unstable angina or non ST segment Elevation Myocardial Infarction (UA/non-STEMI) \[Braunwald class I-III Class B\], Appendix 1).
  • Single vessel disease of the Left Coronary Artery (LCA)
  • One vessel disease of the Right Coronary Artery (RCA)
  • Have a single de novo lesion
  • Older than 18 years and younger than 75 years of age
  • Eligible to undergo PCI on the target vessel

Exclusion Criteria

  • Previous Q-wave myocardial infarction
  • Congestive heart failure with Left ventricular Ejection Fraction \<35%
  • Confirmed pregnancy
  • Anemia to a hemoglobin level \<8.5g/dl
  • Systemic mastocytosis
  • History of known haemorrhagic stroke at any time or any stroke less than or equal to 30 days prior to randomization
  • Severe hypertension (\>180/110mmHG) not adequately controlled by antihypertensive therapy at time of study entry
  • Need for mechanical ventilation
  • Renal impairment: Creatinine \> 1.6mg/dl
  • Known history of COPD with FEV 1s \< 1.0 liter

Arms & Interventions

1

Voluven will be administered at 7.7 ml/min over 15 minutes,followed by Voluven at 7.7 ml/min over 15 minutes

Intervention: Percutaneous Coronary Revascularization

1

Voluven will be administered at 7.7 ml/min over 15 minutes,followed by Voluven at 7.7 ml/min over 15 minutes

Intervention: Voluven

2

HBOC-201 will be administered at 7.7 ml/min over 15 minutes,followed by Voluven at 7.7 ml/min over 15 minutes

Intervention: Percutaneous Coronary Revascularization

2

HBOC-201 will be administered at 7.7 ml/min over 15 minutes,followed by Voluven at 7.7 ml/min over 15 minutes

Intervention: Hemoglobin-Based Oxygen Carrier-201 (HBOC-201)

2

HBOC-201 will be administered at 7.7 ml/min over 15 minutes,followed by Voluven at 7.7 ml/min over 15 minutes

Intervention: Voluven

3

HBOC-201 will be administered at 7.7 ml/min over 15 minutes,followed by HBOC-201 at 7.7 ml/min over 15 minutes

Intervention: Percutaneous Coronary Revascularization

3

HBOC-201 will be administered at 7.7 ml/min over 15 minutes,followed by HBOC-201 at 7.7 ml/min over 15 minutes

Intervention: Hemoglobin-Based Oxygen Carrier-201 (HBOC-201)

Outcomes

Primary Outcomes

Safety

In hospital thrombotic events

Anaphylactic reactions

Inflammatory reactions

Substantial changes to systemic & coronary hemodynamics

Circulatory overload

Renal dysfunction

Untoward drug interaction effects

substantial changes in laboratory parameters

Life threatening cardiac arrhythmias

Other adverse events

Feasibility:

Number of subjects requiring premature discontinuation of study drug for clinical or logistical reasons

Study Sites (6)

Loading locations...

Similar Trials