Temsirolimus Adventitial Delivery to Improve Angiographic Outcomes Below the Knee (TANGO)

Status unconfirmed · Phase 2 · Has a placebo group

Conditions studied: Chronic Limb Ischemia

In brief

This is a prospective, multi-center, randomized, dose escalation study to document the effects of adventitial delivery of temsirolimus (Torisel) after revascularization of lesions below the knee in symptomatic patients with critical limb ischemia (CLI).

Key facts

Study ID

NCT02908035

Run by

Mercator MedSystems, Inc.

People needed

100

Starts

2017-03-03

Expected to finish

2021-09-01

Last updated by the study team

2020-06-11

Who can join

Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Screening Criteria:
• Age ≥18 years and <90 years
• Patient has been informed of the nature of the study, agrees to participate and has signed an IRB approved consent form
• Female patients 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) one month preceding and 12 months following study treatment
• Patient has documented chronic Critical Limb Ischemia (CLI) in the target limb from the distal segment (P3) of the popliteal artery to the ankle joint prior to the study procedure with Rutherford Category 3, 4 or 5
• Life expectancy >1 year in the Investigator's opinion
• Angiographic Criteria:
• Target vessel(s) diameter ≥2 mm and ≤8 mm
• Single or multiple atherosclerotic lesion(s) ≥70% in at least one below-knee popliteal or tibial target vessel including the tibioperoneal trunk that totals up to no greater than 30 cm in length (with no greater than 5 cm length of contiguous intervening normal artery), with possible extension into the popliteal artery distal to the center of the knee joint space (the P3 segment)
• Successful revascularization of the TL with less than 30% residual stenosis, run-off down to the foot and direct in-line flow to any foot wound, if a wound is present at baseline

You may not qualify if…

• Screening Criteria
• Patient is already enrolled in another clinical study of systemic drug therapy or another device study that has not completed its primary endpoint
• Patient unwilling or unlikely to comply with visit schedule
• Patients who are incapable of providing consent and/or incapable of understanding the nature, significance and implications of the clinical trial
• Patient is already receiving or planned to receive systemic immunotherapy, chemotherapy, or steroids (however, inhaled steroids for asthma treatment or topical steroid uses are allowed)
• Patient 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
• Planned major (above the ankle) target limb amputation
• Active foot infection; however, osteomyelitis in the toes or mild cellulitis around the perimeter of gangrene or small ulcers (<25mm) are not exclusions, but osteomyelitis of the metatarsal or more proximal region would be exclusionary
• Inability to receive temsirolimus 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, except for patients with end stage renal disease on chronic hemodialysis
• Stage 3 (per SVS WIfI classification) or worse heel ulcers or heel ulcers that are determined to be primarily neuropathic in nature or non-ischemic in origin
• Angiographic/Procedural Criteria
• Hemodynamically significant inflow lesion (≥50% DS) or occlusion in the ipsilateral iliac, SFA, or popliteal arteries (P1 and P2) 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)
• Target lesion length is >30 cm as measured from proximal normal vessel to distal normal vessel
• Total length of lesions treated during the case (including target lesion, inflow lesions, and other non-target lesions) >30 cm
• 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 or during the previous 2 months within the target lesion
• Previously implanted stent in the TL(s)
• Aneurysm in the target vessel
• Acute thrombus in the target limb
• Failure to cross the TL with a guide wire; however, subintimal wire crossing is allowed
• 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

Where it is running

• Arkansas Heart Hospital — Little Rock, Arkansas, United States
• St. Joseph Hospital of Orange Heart and Vascular Center — Orange, California, United States
• Denver Veterans Administration Hospital — Denver, Colorado, United States
• Advocate Christ Medical Center — Oak Lawn, Illinois, United States
• University Hospital — Cleveland, Ohio, United States
• Einstein Medical Center — Philadelphia, Pennsylvania, United States
• Sanford Research — Sioux Falls, South Dakota, United States
• Baylor College of Medicine — Houston, Texas, United States

Full record on ClinicalTrials.gov

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