Safety/Feasibility Study of HBOC-201 in Amputation at/Below Knee From Critical Lower Limb Ischemia

Biopure

Status and phase: Terminated; Phase 2

Conditions: Peripheral Vascular Disease

Treatments: Drug: 6% Hydroxyethylstarch; Drug: Hemoglobin glutamer 250 - bovine

Study type: Interventional

Funder types: Industry

Identifiers

NCT00300040

BIOSA001/BIOEU001

Details and patient eligibility

About

The purpose of this study is to assess the safety and feasibility of HBOC-201 in increasing adequate wound healing in patients with severe peripheral vascular disease who are undergoing lower limb amputation.

The hypothesis is that HBOC-201 will pass through the partially occluded lesions in the peripheral arteries in the lower extremity and promote the wound healing process by delivering oxygen to the oxygen deprived tissues. This will reduce the incidence of lower limb wound complications at 60 days post-surgery and may reduce the incidence of a second amputation.

Full description

This is a Phase II, single-blinded, prospectively randomized, parallel-group, placebo controlled study that will evaluate the safety and feasibility of HBOC-201 when administered therapeutically to patients with a peripheral vascular occlusive disorder and who are undergoing lower limb amputation due to critical lower limb ischemia. Subjects will be randomized (1:1) to receive either HBOC-201 or a colloid control (HAES-steril® 6%).

Enrollment: 16 patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Subjects ≥ 18 ≤ 75 years of age

• Scheduled amputation at or above ankle joint, or a more proximal location but below or through the knee joint

• Documented severe lower extremity peripheral artery occlusive disease confirmed by clinical symptoms of critical limb ischemia and:

  • Frankly gangrenous tissue that merits amputation or
  • Angiographic evidence of occlusive peripheral artery disease within one month of screening

• Participant or legal representative signs informed consent

• Willingness to follow study instructions and follow-up visits

Exclusion criteria

• No informed consent is obtained
• If medically inappropriate to administer 250 mL colloidal solution daily for 4 consecutive days
• Uncontrolled hypertension (BP > 160/90 mm Hg) despite 2 antihypertensive meds or BP > 180/100 mm Hg if untreated
• Severe liver dysfunction defined by Total Bilirubin > 3 mg/dL or twice the normal limit of serum AST or ALT
• Symptomatic CVD diagnosed w/ in last 6 months or known high grade carotid stenosis
• Any severe or unstable medical condition that might interfere w/ the evaluation of study medication
• Cardiogenic shock (cardiac index < 2 L/min/m2, PCWP > 18 mm Hg)
• Amputation above knee joint or below ankle joint
• Any amputation whereby primary skin closure not technically feasible
• Candidate for percutaneous or surgical revascularization
• Cardiac failure defined by a NY class III/IV or left ventricular ejection fraction < 30%
• Life expectancy < 60 days
• Systemic mastocytosis
• Previously demonstrated beef product allergy
• Myocardial infarction w/ in 30 days
• Participation in another trial w/ in last 30 days
• Woman who is pregnant or breastfeeding
• Amputation with known infection at site of skin closure
• Renal dysfunction requiring dialysis, or serum creatinine level 2.5 mg/dL
• Peripheral vascular occlusion from cardio arterial emboli
• Uncontrolled diabetes blood glucose ≥ 400 mg/dL

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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16 participants in 2 patient groups

1

Experimental group

Description:

Hemoglobin glutamer 250 - bovine

Treatment:

Drug: Hemoglobin glutamer 250 - bovine

2

Active Comparator group

Description:

6% Hydroxyethylstarch

Treatment:

Drug: 6% Hydroxyethylstarch