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New treatment option for Peripheral Artery Disease
Official title Temsirolimus Adventitial Delivery to Improve ANGioplasty and/or Atherectomy Revascularization Outcomes Below the Knee
ClinicalTrials.gov ID: NCT04433572
What this study is testing
What is Temsirolimus?
Temsirolimus is an investigational medicine, given as an injectable medicine, being studied as a potential treatment for peripheral artery disease.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- A multicenter, randomized, double-blind, placebo-controlled trial to evaluate the effect of Temsirolimus Perivascular Injection 0.1 mg/mL on the incidence of ischemia-driven major amputation, clinically driven target lesion revascularization, and clinically relevant target lesion occlusion after revascularization of lesions below the knee in patients with symptomatic Rutherford 3-5 peripheral artery disease. The primary safety endpoint will be gathered at 1-month post-index procedure.
- Phase 3: a large, late-stage study
- Time commitment: about 5 years
- You might receive a placebo (an inactive treatment) instead of the study drug, decided by chance. You may not know which one you got.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Pre-procedural:
- Participant has signed and dated informed consent, is capable of understanding the nature, significance and implications of the clinical trial, and...
- Participant is male or female, aged 18 years or older.
- If participant is female and of reproductive potential: agreement to use a highly effective contraception (abstinence is acceptable) for at least 90...
- Participant has severe claudication (Rutherford 3) or chronic limb-threatening ischemia (CLTI) (Rutherford 4-5) in the Target Limb...
You likely can't join if
- Pre-procedural:
- Participant is already enrolled in another clinical study of systemic or local vascular drug therapy or a vascular device study that has not...
- Participant is pregnant, nursing, or planning to become pregnant during the first 12 months after their enrollment in the study.
- Participant has presence of another anatomic or comorbid condition, or other medical, social, or psychological condition that, in the investigator's...
- Incapacitated individuals, defined as persons who are mentally ill, mentally handicapped, or individuals without legal authority, are excluded from...
- Participant has a life expectancy of ≤1 year.
See the full eligibility criteria
Who can join
- Pre-procedural:
- Participant has signed and dated informed consent, is capable of understanding the nature, significance and implications of the clinical trial, and is willing to comply with all study procedures and follow-up visits for...
- Participant is male or female, aged 18 years or older.
- If participant is female and of reproductive potential: agreement to use a highly effective contraception (abstinence is acceptable) for at least 90 days after study treatment.
- Participant has severe claudication (Rutherford 3) or chronic limb-threatening ischemia (CLTI) (Rutherford 4-5) in the Target Limb. Angiographic/Procedural:
- Participant has up to two de novo or restenotic Qualified Target Lesions meeting the following criteria, each based on the Investigator's visual assessment. Target Lesions should be considered separate if they are...
- ≥70% diameter stenosis anywhere within the Target Lesion or ≥50% diameter stenosis spanning at least 10 cm of length.
- Reference (normal) vessel diameter ≥2 mm and ≤8 mm. Location
- Any lesion chosen as a Target Lesion is in or spans at least one below-knee popliteal (P3 segment), tibial, or peroneal artery and is a culprit for dominant disease symptoms based on Investigator's assessment.
- ≥50% of the Target Lesion length is below the knee joint space (\<50% of Target Lesion length may extend above the midline of the knee joint space).
- ≥10 mm away from any previously placed stent or graft.
- A Target Lesion may cross an ostium of another artery (i.e. pass a bifurcation) but may only include one of the two branches. (Notes: Investigator should choose the dominant lesion for Target Lesion. Bifurcated lesions...
- ≤30 cm in cumulative length from most proximal to most distal normal segment bounding the Target Lesion(s).
- A single Target Lesion may be comprised of multiple lesions or multifocal lesions (i.e. tandem lesions) if there is no continuous normal segment \>10cm in length within the Target Lesion.
- Target Lesion may be in a vessel with another Target Lesion or above-knee non-target lesion if it is \>10 cm away.
- Participant receives successful revascularization, based on the following Investigator visual assessments:
- Target Lesion and any treated non-target lesion in a Target Vessel or its inflow has \<30% residual stenosis, outflow has \<50% stenosis, and there is no flow-limiting dissection or perforation after treatment in an...
- Participant has distal run-off into the foot with a patent named pedal artery.
What rules you out
- Pre-procedural:
- Participant is already enrolled in another clinical study of systemic or local vascular drug therapy or a vascular device study that has not completed its primary endpoint, including prior enrollment in this study.
- Participant is pregnant, nursing, or planning to become pregnant during the first 12 months after their enrollment in the study.
- Participant has presence of another anatomic or comorbid condition, or other medical, social, or psychological condition that, in the investigator's opinion, could limit the participant's ability to complete the...
- Incapacitated individuals, defined as persons who are mentally ill, mentally handicapped, or individuals without legal authority, are excluded from the study population.
- Participant has a life expectancy of ≤1 year.
- Participant received in the prior 2 months, is currently receiving, or is planned to receive systemic immunosuppressive therapy, immunotherapy or chemotherapy.
- Participant has platelet count \ 700,000 cells per microliter, or hemoglobin \< 7.5 g/dL.
- Participant is unable to receive H1 antihistamine, temsirolimus or iodinated contrast medium due to labeled contra-indications or known sensitivity reactions except for contrast allergies for which adequate prophylaxis...
- Participant has a CNS tumor.
- Participant has had a myocardial infarction within the 30 days prior to study procedure.
- Participant has had a cerebrovascular accident within the 90 days prior to the study procedure.
- Participant has had an intracerebral hemorrhage within the 1 year prior to the study procedure.
- Participant has had any vascular surgical or endovascular procedure performed within the 30 days prior to the Index Procedure or planned within the 30 days after the Index Procedure; allowable exceptions to this...
- Procedures performed during the same setting as the Index Procedure.
- Prior staged revascularization in the Target Limb but not the Target Lesion (e.g. for inflow revascularization) within the 30 days prior to the Index Procedure.
- Participant has a patent, previously implanted bypass graft within 3 cm of the Target Lesion.
- Participant is bedridden or unable to walk (with assistance is acceptable). Participants in wheelchair who are able to mobilize on their own can be enrolled.
- Participant has a planned major (above the ankle) amputation in the Target Limb.
- Participant has had any amputation to the ipsilateral extremity other than the toe or forefoot, or has had major amputation to the contralateral extremity \< 1 year prior to index procedure and is not independently...
- Participant has signs or symptoms of advanced limb infection or septicemia (fever \> 38.5℃, white blood cell count \> 15,000 cells per microliter, hypotension) at the time of assessment. Osteomyelitis of the phalanges...
- Participant has extensive tissue loss salvageable only with complex foot reconstruction or non-traditional amputations (e.g. Chopart or Lisfranc extending more proximal than a traditional transmetatarsal amputation)...
- Osteomyelitis that extends proximal to the metatarsal heads. Osteomyelitis limited to the phalanges or metatarsal heads is acceptable for enrollment.
- Any of the following involving the plantar skin of the forefoot, midfoot, or heel that cannot be effectively removed with a transmetatarsal amputation: i) Gangrene. ii) Deep ulcer (penetrating deeper than the dermis to...
- Participant has a bilirubin level of \>1.5xULN (upper limit of normal range).
- Participant has an estimated glomerular filtration rate (eGFR) less than 30 mL/min, except for patients with end stage renal disease on stable, chronic dialysis. Angiographic/Procedural:
- Participant has severe, advanced atherosclerotic peripheral artery disease (treated or left untreated) in the Target Limb which, in the opinion of the Investigator, has limited likelihood of a successful outcome.
- Participant has stenotic lesions, flow limiting dissection, or complication in any of the inflow or outflow vessels in the flow path of the Target Lesion, left untreated or after treatment, with residual stenosis \>30%...
- Participant receives or has received external radiation therapy to the target limb, vascular brachytherapy, cryotherapy, or drug-coated balloon (DCB) as part of the Target Lesion treatment during the index procedure or...
- Participant has been treated with a non-resorbable stent/scaffold in the Target Lesion in a prior setting (i.e. in-stent restenosis) or a bioresorbable scaffold in the Target Lesion in the previous 12 months.
- Participant has a severe (Type C or worse) dissection within the Target Lesion after revascularization but prior to Bullfrog drug delivery.
- Participant has an untreated aneurysm in the iliac, common femoral, superficial femoral, popliteal, or Target Vessel of the ipsilateral limb.
- Participant has visible thrombus requiring thrombolysis, percutaneous thrombectomy, or other treatment for acute limb ischemia of the Target Limb.
- Participant has angiographic evidence of thromboembolism or atheroembolism in the ipsilateral extremity upon completion of the intervention. (Pre- and post-angiographic imaging must confirm the absence of emboli in the...
- Participant has a Target Lesion that cannot be crossed with a guide wire; however, subintimal wire crossing is allowed.
- Participant has heavy calcification at Target Lesion, which in the judgment of the investigator would prevent penetration of the Micro-Infusion Device needle through the vessel wall across the majority of the Target...
The study team makes the final eligibility decision.
Where it's taking place
- Houma, Louisiana, United States
- Dallas, Texas, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The study runs about 5 years per participant, based on its public description. The team confirms the exact schedule and number of visits before you enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Houma, Louisiana, United States; Dallas, Texas, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.