VEGF Gene Transfer for Critical Limb Ischemia

Phase 1

Completed

• Conditions: Critical Limb Ischemia; Ischemia; Leg Ulcer

• Registration Number: NCT00304837
• Lead Sponsor: Losordo, Douglas, M.D.

Brief Summary

The purpose of this gene therapy study is to evaluate the safety and efficacy of intramuscular gene transfer using Vascular Endothelial Growth Factor (VEGF) or placebo in patients with moderate to high-risk Critical Limb Ischemia (a condition in which there is poor blood circulation in the leg). This trial will assess whether VEGF improves rest pain and/or heals ulcers in the legs of patients with peripheral artery disease (blockages in leg arteries.)

VEGF is DNA, or genetic material that will be injected into the leg muscles on three separate occasions, each 2 weeks apart. Once the DNA is in the leg, it directs the cells of the artery wall to increase its production of VEGF, which has been shown to cause new blood vessels to grow. This experimental therapy is designed to grow new blood vessels around blockages in the leg arteries.

The total length of participation in this study is approximately 1 year and will require approximately 8 clinic visits within that year. Following enrollment in the study, testing may be done for cancer screening, blood work, physical exams, vascular testing and eye exams. There is no charge for any testing or office visits required by the study.

This study has been approved by the Food and Drug Administration (FDA).

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2006-03-16
• Study First Submitted QC: 2006-03-16
• Study First Posted: 2006-03-20
• Status Verified: 2008-04
• Study Completion: 2008-04
• Last Update Submitted: 2010-10-18
• Last Update Posted: 2010-10-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Be at least 21 years old
• Have critical limb ischemia
• Have severe blockages in at least one artery in the affected leg as demonstrated by an angiogram
• Have nonhealing leg ulcers and/ or have severe rest pain secondary to a severely decreased blood flow
• Agree to participate in follow-up.

Exclusion Criteria

• Have any evidence of malignant neoplasms (other than non-melanoma skin cancer or in situ carcinoma) within the last 5 years
• Be pregnant or lactating
• Have a history of alcohol or drug abuse within 3 months of screening
• Have advanced (Rutherford Category 6) critical limb ischemia, characterized by extensive tissue loss or gangrene
• Have osteomyelitis
• Have undergone successful aortic or lower extremity surgery, angioplasty, or lumbar sympathectomy within the 2 months preceding screening
• Be a suitable candidate for surgical or endovascular revascularization in the limb in which treatment is proposed
• Subjects in whom arterial insufficiency in the lower extremity is the result of a non-atherosclerotic disorder

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Trial Locations

Locations (3)

The Minneapolis Heart Institute at Abbott Northwestern Hospital; 🇺🇸 Minneapolis, Minnesota, United States

Cardiology PC; 🇺🇸 Birmingham, Alabama, United States

Caritas St. Elizabeth's Medical Center; 🇺🇸 Boston, Massachusetts, United States