SDF1 Plasmid Treatment for Patients With Peripheral Artery Disease (STOP-PAD)
Peripheral Arterial Disease
About this trial
This is an interventional treatment trial for Peripheral Arterial Disease
Eligibility Criteria
Major Inclusion Criteria:
- Age ≥18
- Currently receiving standard of care wound treatment (>2 weeks) for chronic wounds or gangrene including as indicated: debridement, pressure offloading, infection control, and/or maintenance of a moist wound environment.
- Diagnosis of advanced PAD with tissue loss (ulceration and/or dry gangrene) on the foot of the index leg with an ulcer size of at least 0.5 cm2 and <25 cm2. Index wounds on the heel must be <10 cm2 that cannot be probed to bone, have exposed bone or osteomyelitis.
Post revascularization intervention inclusion criteria include an attempt at open bypass grafting or endovascular intervention of a popliteal/infrapopliteal lesion(s) on the same leg that has tissue loss without significant improvement in TBI post intervention. The following will be accepted as demonstrating a lack of post intervention toe brachial index (TBI) improvement:
- TBI ≤ 0.51or;
- Toe pressure ≤50 mmHg with flat or dampened wave forms or;
- Skin Perfusion pressure ≤40 mmHg at mid foot level or;
- TcPO2 ≤40 mmHg
- Subjects willing to forgo treatment with hyperbaric oxygen, nerve stimulation or sympathectomy for the treatment of advanced PAD from time of consent to 6 months following the initial injection of study drug
Major Exclusion Criteria:
- Previous major amputation of the leg to be treated or planned major amputation or transmetatarsal amputation within the first month following enrollment.
- Only a short segment superficial femoral artery lesion - consistent with Inter-Society Consensus for the Management of Peripheral Arterial Disease (TASC II) A or B category, and no infrapopliteal disease
- Staged or planned intervention in the index leg within 30 days after the index procedure
- Acute limb-threatening ischemia, trauma, known non-atherosclerotic vascular disease
- Non-salvageable limb defined as major tissue loss and an unsalvageable foot;
- Wounds that have decreased in size by >50% between the Screening visit and Day 0.
- If patient has active infection of the index limb that is being treated, and, in the opinion of treating physician, will not lead to an amputation within the next 3 months, the patient can be enrolled.
- Inability to safely perform a revascularization procedure due to uncontrolled diabetes or other medical condition.
- Presence of any other condition that, in the opinion of the investigator, might compromise any aspect of the trial
Sites / Locations
- Cardiovascular Associates of the Southeast
- UC DavisRecruiting
- Cedars-Sinai Heart InstituteRecruiting
- MedStar Georgetown UH
- Morton Plant Hosptial - BaycareRecruiting
- Mount Sinai Medical CenterRecruiting
- St. Joseph's HospitalRecruiting
- NorthwesternRecruiting
- RUMCRecruiting
- Cardiovascular Institute of the SouthRecruiting
- St. John Hospital and Medical CenterRecruiting
- MayoRecruiting
- Cardiology Associates ResearchRecruiting
- St. Luke's Mid America Heart InstituteRecruiting
- Holy Name Medical CenterRecruiting
- UNCRecruiting
- NC Heart and Vascular ResearchRecruiting
- Summa HealthRecruiting
- Cleveland ClinicRecruiting
- Metro HealthRecruiting
- University HospitalsRecruiting
- Lifespan Health SystemRecruiting
- VCURecruiting
- Medical College of WisconsinRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Active Comparator
Placebo Comparator
Active Comparator
Placebo Comparator
8 mg JVS-100
8 mg placebo
16 mg JVS-100
16 mg placebo
Biological/Vaccine: JVS-100 Injection Intramuscular Injection
Biological/Vaccine: Placebo Injection Intramuscular Injection
Biological/Vaccine: JVS-100 Injection Intramuscular Injection
Biological/Vaccine: Placebo Injection Intramuscular Injection