Summary

for people ages 18-85 (full criteria)
at San Francisco, California and other locations
study started
estimated completion

Description

Summary

This is a prospective, multi-center, pilot feasibility study to document the effects of adventitial delivery of temsirolimus or temsirolimus with dexamethasone sodium phosphate injection, USP, after revascularization of femoropopliteal lesions in symptomatic patients with moderate to severe claudication (Rutherford 2-3) or critical limb ischemia (CLI) with rest pain (Rutherford 4). Subjects will be followed for up to 60 months post index procedure.

Details

To begin to assess the safety and effectiveness of Bullfrog Micro-Infusion Device adventitial deposition of temsirolimus or temsirolimus with dexamethasone in maintaining luminal patency and composite safety endpoints in patients with clinical evidence of moderate to severe claudication or critical limb ischemia with rest pain after revascularization of one or more angiographically significant lesion(s) in superficial femoral or popliteal arteries.

Keywords

Peripheral Arterial Disease Peripheral Vascular Diseases Sirolimus Dexamethasone Dexamethasone acetate Everolimus Dexamethasone 21-phosphate BB 1101 Temsirolimus Temsirolimus and dexamethasone sodium phosphate

Eligibility

For people ages 18-85

Inclusion Screening Criteria:

  • Age ≥18 years and ≤85 years at study enrollment
  • Subject has been informed of the nature of the study, agrees to participate and has signed an IRB-approved consent form
  • Subject is ambulatory
  • Female subjects of childbearing potential have a negative pregnancy test ≤7 days before the procedure and are willing to use a highly effective method of birth control (See Section 12.2) for one month preceding and 12 months following study treatment
  • Subject has documented moderate to severe claudication (Rutherford 2-3) or Critical Limb Ischemia (CLI) with rest pain (Rutherford 4) in the target limb due to arterial stenosis within the superficial femoral and/or popliteal artery
  • Life expectancy >2 years in the Investigator's opinion Angiographic Criteria (Target Lesion Definition)
  • Target vessel reference diameter ≥3 mm and ≤8 mm
  • Single or multiple de novo atherosclerotic or restenotic lesion(s) with ≥70% narrowing in the superficial femoral or popliteal artery meeting the following criteria:
  • The target lesion must be ≤20 cm in total length
  • The target lesion does not have more than 5 cm of contiguous length of intervening normal artery
  • The target lesion does not cross into the common femoral artery or tibeoperoneal trunk
  • The target lesion is located at least 10 mm away from any previously placed stent or graft
  • Successful wire crossing (sub-intimal is allowed) and revascularization by balloon angioplasty of the target lesion with less than 30% residual stenosis and run-off in at least one patent vessel into the foot

Exclusion Screening Criteria:

  • Subject is already enrolled in another clinical study of systemic drug therapy or another device study that has not completed its primary endpoint
  • Subject unwilling or unlikely to comply with visit schedule
  • Subjects who are incapable of providing consent and/or incapable of understanding the nature, significance and implications of the clinical trial
  • Subject is already receiving, has received in prior 2 months, or is planned in the 6 months after index procedure to receive systemic immunotherapy, chemotherapy, or systemic steroids (however, steroid pre-treatment for contrast allergy, inhaled steroids for asthma treatment or topical steroid uses are allowed)
  • Subject is receiving chronic anticoagulation therapy e.g. warfarin (note: chronic antiplatelet therapy, e.g. aspirin and clopidigrel, and procedural anticoagulation therapy, e.g. heparin or bivalirudin, are allowed)
  • Subject has a bilirubin level of >1.5xULN
  • Recent (<30 days prior to study procedure) myocardial infarction
  • Cerebrovascular accident <60 days prior to the study procedure or any history of intracerebral hemorrhage
  • Any surgical or endovascular procedure (not including staged revascularization in the target limb, e.g. inflow revascularization prior to index procedure or below-knee revascularization after the index procedure) performed within 14 days prior to the index procedure or planned within 30 days post index procedure
  • Planned amputation in the target limb
  • Active foot infection or ischemic foot wound
  • Inability to receive temsirolimus, dexamethasone or iodinated contrast medium due to labeled contra-indications or known sensitivity reactions
  • Estimated glomerular filtration rate (eGFR, calculated from serum creatinine using an isotope dilution mass spectrometry (IDMS)-traceable equation) less than 30 mL/min Angiographic/Procedural Criteria
  • Hemodynamically significant inflow lesion (≥50% DS) or occlusion in the ipsilateral iliac artery in which there is failure to successfully treat and obtain a <30% residual stenosis post-revascularization, with bailout stenting as needed (in-flow lesions should be treated prior to treating the target lesion)
  • Prior stent placement in target lesion (i.e., in-stent restenosis)
  • Target lesion restenosis of any kind within 6 months of a prior intervention
  • Use of alternative therapy, e.g. radiation therapy, drug-eluting stents (DES) or drug-eluting balloon/drug-coated balloons (DEB/DCB) as part of the target lesion treatment during the index procedure or during the previous 12 months
  • Use of atherectomy devices in the target lesion during the index procedure
  • Aneurysm in the target vessel
  • Acute thrombus in the target limb
  • Heavy eccentric or concentric calcification at target lesion, which in the judgment of the investigator would prevent penetration of the Micro-Infusion Device needle through the vessel wall

Locations

  • San Francisco VA Medical Center
    San Francisco California 94121 United States
  • St. Joseph Hospital of Orange Heart and Vascular Center
    Orange California 92868 United States

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
Mercator MedSystems, Inc.
ID
NCT03942601
Phase
Phase 2
Study Type
Interventional
Last Updated