Safety and Efficacy Study Using Gene Therapy for Critical Limb Ischemia

In the absence of revascularization options, most patients with CLI require amputation
within 6 months. Patients requiring major amputation face a diminished quality of life, an
unfavorable natural history and need extensive resources for their post-amputation
rehabilitation and course. The 1-year amputation-free survival rate for patients diagnosed
with CLI is 45%; the mortality rate is approximately 25% and may be as high as 45% in those
who have undergone amputation. Management of this end-stage disease process consumes a
significant amount of healthcare resources. Clearly, new therapeutic approaches are
required.

Hepatocyte growth factor (HGF) has been shown to be a potent angiogenic growth factor
stimulating the growth of endothelial cells and migration of vascular smooth muscle cells.
Because of its pluripotent capabilities, increasing the availability of HGF in ischemic
tissues to achieve therapeutic angiogenesis has been a growing area of research.

This study will use VM202, which is a DNA plasmid that contains novel genomic cDNA hybrid
human HGF coding sequence (HGF-X7) expressing two isoforms of HGF, HGF 728 and HGF 723. As
there are currently no approved drugs that can reverse CLI and as most patients have
exhausted surgical and endovascular intervention options, inducing angiogenesis in the
affected limb with VM202 may result in an increase in tissue perfusion, which, in turn
improve wound healing, reduce pain and improve limb salvage rates.

Inclusion Criteria:

- Male or female, between 18 and 90 years of age;

- Diagnosis of critical limb ischemia (Rutherford Class 4 or 5), including:

- A resting ankle systolic pressure (in either the dorsalis pedis or posterior
tibial arteries) of ≤ 70 mmHg in the affected limb; or

- A resting toe systolic pressure of ≤ 50 mmHg in the affected limb; or

- For patients in which measurement of ankle systolic pressure is not feasible
(e.g. vessel calcification and non-compressibility); TcPO2 ≤ 30 mmHg;

- Poor or suboptimal candidate for bypass graft surgery or percutaneous angioplasty;

- Pain at rest, and/or ischemic ulcers, and/or focal gangrene (< 3 cm2) for a minimum
of 2 weeks,

- Significant stenosis (≥ 75%) of one or more of the following arteries: superficial
femoral, popliteal, or two or more infra-popliteal arteries as verified by
angiography within 12 months prior to enrollment;

- Be willing to maintain current drug therapy for peripheral arterial disease
throughout the course of the study including an anti-platelet and statin treatment
unless not tolerated;

- Clinically stable on optimized medical regimen for >30 days

- Be capable of understanding and complying with the protocol and signing the informed
consent document prior to being subjected to any study related procedures;

- Women who are surgically sterile or at least 1 year postmenopausal or who have been
practicing adequate contraception for at least 12 weeks prior to entering the study.
If the subject is of child-bearing potential, she must have a negative urine
pregnancy test result prior to study enrollment and must agree to repeat pregnancy
screening tests during the study. If the subject or the subject's partner(s) is of
child bearing potential, the subject and the subject's partner(s) must agree to use a
"double barrier" method of birth control while participating in this study.

Exclusion Criteria:

- Subjects who have undergone a successful revascularization procedure or sympathectomy
within 12 weeks prior to study entry. A clinically unsuccessful revascularization
procedure is defined as one in which:

- the target vessel re-occludes (≥50%, as verified by a second angiogram. Duplex
ultrasonography can be used to determine vessel patency if the patient cannot
tolerate a second angiogram), or

- the target vessel remains patent, but there is no resolution of symptoms 6 weeks
after the procedure (e.g. no evidence of ulcer healing, no improvement in
pressures, no reduction in resting pain);

- Subjects that will require an amputation in the target leg within 4 weeks of
randomization;

- Subjects with evidence of active infection (e.g., cellulitis, osteomyelitis) or deep
ulceration exposing bone or tendon in the extremity planned for treatment;

- Heart Failure with a NYHA classification of III or IV;

- Stroke (NIH scale >2) or myocardial infarction within last 3 months;

- Unstable angina

- Uncontrolled hypertension defined as sustained systolic blood pressure (SBP) > 200
mmHg or diastolic BP (DBP) > 110 mmHg at baseline/screening evaluation;

- Ophthalmologic conditions pertinent to proliferative retinopathy or conditions that
preclude standard ophthalmologic examination;

- Inflammatory disorder of the blood vessels (inflammatory angiopathy, such as
Buerger's disease);

- Subjects with advanced liver disease including decompensated cirrhosis, jaundice,
ascites or bleeding varices;

- Subjects currently receiving immunosuppressive medications chemotherapy, or radiation
therapy;

- Positive HIV or HTLV at screening;

- Active Hepatitis B or C infection as determined by Hepatitis B surface antibody
(HBsAb), Hepatitis B core antibody (IgG and IgM; HBcAb), Hepatitis B surface antigen
(HBsAg) and Hepatitis C antibodies (Anti-HCV), at Screening;

- Specific laboratory values at Screening including: Hemoglobin < 8.0 g/dL, WBC < 3,000
cells per microliter, platelet count <75,000/mm3, AST and/or ALT > 3 times the upper
limit of normal or any other clinically significant lab abnormality which in the
opinion of the investigator should be exclusionary;

- Patients with a recent history (< 5 years) of or new screening finding of malignant
neoplasm except basal cell carcinoma or squamous cell carcinoma of the skin (if
excised and no evidence of recurrence); patients with family history of colon cancer
in any first degree relative are excluded unless they have undergone a colonoscopy in
the last 12 months with negative findings;

- Elevated PSA unless prostate cancer has been excluded;

- Subjects with any co- morbid conditions likely to interfere with assessment of safety
or efficacy or with an estimated life expectancy of less than 6 months

- Subjects requiring > 81 mg daily of acetylsalicylic acid; If > 81 mg are taken at
screening, subjects may be enrolled if willing/able to switch to another medication;

- Subjects requiring regular COX-2 inhibitor drug(s) or high dose steroids (excepting
inhaled steroids);

- Major psychiatric disorder in past 6 months;

- History of drug or alcohol abuse / dependence in the past 2 years;

- Use of an investigational drug or treatment in past 12 months; concurrent
participation in investigational protocol or unapproved therapeutics and

- Unable or unwilling to give informed consent.