The primary objective is to evaluate safety and tolerability of single and repeated administrations of escalating doses of NV1FGF administered intramuscularly in patients with severe Peripheral Artery Occlusive Disease (PAOD), (Rutherford's Grade II, category 4 or Grade III, category 5 and 6). Secondary objectives are: * To determine the biological activity of NV1FGF on collateral artery development. * To evaluate the activity of NV1FGF on hemodynamic and clinical parameters.
Screening period of 30 days before dosing. Patients receive a single administration or repeated (2) administrations (with a 2-week interval) of NV1FGF. Patients are then followed for a period of 6 months
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
51
Pharmaceutical form:solution Route of administration: intramuscular
Unnamed facility
Minneapolis, Minnesota, United States
Unnamed facility
Tempere, Finland
Safety assessment (adverse events, physical examination,vital signs,ECG, laboratory tests...)
Time frame: 12 weeks
hemodynamic parameters (TcPO2, Ankle Brachial Index, Toe Brachial Index, pulse volume recording) and angiography
Time frame: 12 weeks
ulcers healing assessment (length, width, type, depth)
Time frame: 12 weeks
pain assessment (self-administered visual analog scale)
Time frame: 12 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.