Study of HGF Via Plasmid Vector to Improve Perfusion in Critical Limb Ischemia

Peripheral Vascular Disease Clinical Trial

Official title:

A Phase II Double-Blind, Randomized, Placebo-Controlled Study to Assess the Safety and Efficacy of AMG0001 to Improve Perfusion in Critical Leg Ischemia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00060892
• Other study ID #: AG-CLI-0202
• Status: Completed
• Phase: Phase 2
• First received: May 15, 2003
• Last updated: January 9, 2008
• Start date: April 2003
• Est. completion date: January 2007

Study information

• Verified date: January 2008
• Source: AnGes
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The primary purpose of this study was to assess the overall safety of different dose regimens of AMG0001 (HGF transferred via plasmid vector) as well as evaluate the improvement of blood perfusion in subjects with critical limb ischemia (CLI). This study also evaluated the improvement in wound healing without adverse effects on the quality of life, as well as the potential reduction of amputation, mortality and rest pain in the CLI population.

Description:

The primary goal of this study was to assess the safety of AMG0001, detect potential angiogenesis response to AMG0001 treatment and to correlate these changes to clinical endpoints dependent upon improvement in tissue perfusion for relief of CLI complications. The objectives of this study were to:

• Assess the overall safety of different exposure regimens of AMG0001 in the CLI subject population.

• Evaluate the potential effect of angiogenesis associated with different doses and dose regimens of AMG0001 as measured by improvement in tissue perfusion.

• Evaluate the activity of different exposure regimens of AMG0001 to benefit clinical outcomes of reduction of amputation and mortality, wound healing, rest-pain reduction and improvement in subject's ability to function without adverse consequences on quality of life.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 104
• Est. completion date: January 2007
• Est. primary completion date: May 2006
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 40 Years and older

Eligibility

Inclusion Criteria:

• Subjects will have one or more clinical indications diagnostic of CLI such as: distal extremity pain at rest that requires the subject to use analgesics for >2 weeks; or peripheral ischemic ulcer(s); or areas of gangrene.

• The subject will have a TcPO2 of </= 40 mmHg.

• Subjects will have one or both of the following hemodynamic indicators of severe peripheral arterial occlusive disease: (a) Ankle systolic pressure of </= 70 mmHg; (b)Toe systolic pressure </= 50 mmHg.

• The subject is a poor candidate for standard revascularization treatment options for peripheral arterial disease, based on inadequate bypass conduit, unfavorable anatomy, or poor operative risk.

• Subject has signed an informed consent form either directly or through a legally authorized representative

• If female, the subject must be (a) at least one year post-menopausal, or (b) surgically sterile, or (c) if the subject is of child-bearing potential, she must have been practicing contraception for at least 12 weeks prior to entering the study.

• If subject is of reproductive potential, he or she must be using an accepted and effective (barrier) form of birth control during the study.

• Subjects will be on a statin and an anti-platelet agent as part of their standard of care and must be stable on these regimens for at least 4 weeks prior to treatment.

Exclusion Criteria:

• Subjects, who in the opinion of the investigator, have a vascular disease prognosis that indicates they would require a major amputation (at or above the ankle) within 4 weeks of start of treatment.

• Subjects with a diagnosis of Buerger's disease (Thromboangitis Obliterans).

• Subjects with hemodynamically significant aorto-iliac occlusive disease.

• Subjects who have had a revascularization procedure within 12 weeks prior to treatment initiation that remains patent. Revascularization procedures that are evidenced to have failed for >2 weeks prior to treatment initiation are acceptable.

• Subjects who require a change in their hypertension medication as part of their standard of care within 4 weeks prior to treatment.

• Evidence or history of malignant neoplasm (clinical, laboratory or imaging), except for basal cell carcinoma of the skin.

• Subjects who have proliferative diabetic retinopathy or severe, non-proliferative retinopathy

• Subjects with end stage renal disease (ESRD) defined as significant renal dysfunction evidenced by a creatinine of > 2.5, or receiving chronic hemodialysis therapy.

• A subject who has hepatic cirrhosis, viral hepatitis, or is HIV positive.

• Subjects with a clinically significant liver enzyme abnormality (i.e., AST or ALT more than two times the upper limit of normal and/or bilirubin more than 50% the upper limit of normal).

• Subjects requiring the use of hyperbaric oxygen treatment for wound healing during the screening and 6 month follow-up period.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Arterial Occlusive Disease
• Arterial Occlusive Diseases
• Ischemia
• Peripheral Arterial Disease
• Peripheral Vascular Disease
• Peripheral Vascular Diseases
• Vascular Diseases

Intervention

Genetic:
• HGF plasmid
Intramuscular injections into index leg on Days 0, 14, and 28

Locations

Country	Name	City	State
United States	American Cardiovascular Research Institute	Atlanta	Georgia
United States	Cardiology, P.C.	Birmingham	Alabama
United States	University of Chicago Hospitals	Chicago	Illinois
United States	The Lindner Clinical Trial Center	Cincinnati	Ohio
United States	The Cleveland Clinic Foundation	Cleveland	Ohio
United States	Pitt County Memorial Hospital	Greenville	North Carolina
United States	Baylor College of Medicine	Houston	Texas
United States	The Care Group, LLC	Indianapolis	Indiana
United States	Dartmouth - Hitchcock Medical Center	Lebanon	New Hampshire
United States	Central Arkansas Veteran's Healthcare System	Little Rock	Arkansas
United States	Cedars-Sinai Medical Center	Los Angeles	California
United States	The Ochsner Heart and Vascular Institute	Metairie	Louisiana
United States	Minneapolis Heart Institute Foundation	Minneapolis	Minnesota
United States	Diabetes Foot and Ankle Center	New York	New York
United States	NYPH-NY Weill Cornell Medical Center	New York	New York
United States	University of Oklahoma Health Sciences Center	Oklahoma City	Oklahoma
United States	Basptist Hospital	Pensacola	Florida
United States	University of Rochester	Rochester	New York
United States	Peripheral Vascular Associates	San Antonio	Texas
United States	Falk Cardiovascular Research Center	Stanford	California
United States	University of South Florida College of Medicine	Tampa	Florida
United States	Jobst Vascular Center	Toledo	Ohio
United States	Medical College of Ohio	Toledo	Ohio
United States	VA Medical Center Surgical Service (112)	Washington	District of Columbia

Sponsors (1)

Lead Sponsor	Collaborator
AnGes

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tissue perfusion as measured by TcPO2		6 months	No
Secondary	Ulcer healing		6 months	No