Angiogenesis and Blood Perfusion Effect of HGF Gene Therapy in PAD Patients

Beijing Northland Biotech

Status and phase: Enrolling; Phase 3

Conditions: Peripheral Artery Disease

Treatments: Drug: NL003; Drug: Placebo

Study type: Interventional

Funder types: Industry

Identifiers

NCT05968118

NL003-PAD-III-3

Details and patient eligibility

About

The purpose of this study is to evaluate whether PET/CT-RGD or MIBI can be used for the angiogenesis assessment of NL003 in PAD patients.

Full description

Hepatocyte growth factor (HGF) gene therapy has been shown to be a potential choice for CLI patients without surgical option. NL003, 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. Animal studies showed that NL003 inducing angiogenesis in the affected limb and result in an increase in tissue perfusion. Our previous phase II clinical trial has suggested the successful limb-salvaging capacity of NL003 in treatment of patients with CLTI.

In this study we will use 68Ga RGD PET/CT and 99mTc MIBI SPECT imaging methods to evaluate the effect of NL003 on angiogenesis and lower limb blood flow perfusion during the treatment of chronic lower limb ischemia, and evaluated the effectiveness and safety of the drug. The subjects will be randomly divided into the investigational drug group and the placebo group in a 1:1 ratio. NL003 or placebo will be injected into the muscle of the affected limb on D0, D14 and D28, 0.5mg/0.5mL/site, total 8mg, 32 sites. PET/CT will be measured on D14, D42 before drug administration, MIBI SPECT imaging will be collected on D60.

Enrollment: 36 estimated patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. 18-80 years, diagnosed with chronic lower limb ischemia;
2. According to DSA or CTA，severe stenosis (≥70%) or occlusion of one or more branches of superficial femoral artery, popliteal artery, anterior tibial artery, posterior tibial artery, and peroneal artery.
3. Patients with obvious symptoms of lower limb ischemia, including severe claudication, resting pain, ulcers, or gangrene.
4. Agree to use appropriate contraceptive methods during the trial; Female subjects of reproductive age, blood pregnancy test negative.
5. Signing the informed consent.
6. Can complete PETCT-RGD check and MIBI check;

Exclusion criteria

1. The foot or lower limb infection cannot be controlled, and amputation may be accepted within 3 months.
2. Those with cerebral infarction, cerebral hemorrhage, heart failure, unstable angina, acute myocardial infarction, and serious arrhythmia within 3 months;
3. Tumor patients diagnosed with malignant tumor or suspected of having malignant tumor after tumor screening;
4. Main iliac artery stenosis ≥ 70%;
5. Refractory hypertension (taking three or more antihypertensive drugs, systolic blood pressure ≥ 180mmHg or diastolic blood pressure ≥ 110mmHg);
6. Anti HIV antibody positive person, anti hepatitis C antibody positive person and RNA positive person, hepatitis B surface antigen positive person (if the subject is HBsAg positive, and judging by peripheral blood HBV DNA, the researcher believes that the subject is in a stable period of chronic hepatitis B, which will not increase the risk of the subject, the subject can be selected)
7. Patients with poor blood glucose control after treatment (HbA1c>10%);
8. Persons allergic to contrast medium
9. The investigator believes that the patient's complications affect the evaluation of safety and effectiveness, or the expected survival period is less than 12 months;
10. Those who regularly drink more than 14 units of alcohol (1 unit=360 mL beer or 45 mL liquor or 150 mL wine with 40% alcohol) or drug abusers within 12 months before signing the informed consent form;
11. Acute lower limb ischemia or acute aggravation of chronic lower limb ischemia;
12. Those who received vascular reconstruction of the affected limb within 4 weeks before the informed consent form and whose blood supply improved after the operation
13. Serious liver or kidney disease or severe anemia judged by the investigator;
14. Those who cannot correctly describe symptoms and emotions;
15. Those who participated in other clinical trials within 3 months before signing the informed consent form.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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36 participants in 2 patient groups, including a placebo group

investigational product

Experimental group

Description:

Patients in this treatment group will receive 8mg NL003 respective in D0、14、28

Treatment:

Drug: NL003

Placebo

Placebo Comparator group

Description:

Patients in this group will receive normal saline respective in D0、14、28

Treatment:

Drug: Placebo