Firehawk Rapamycin Target Eluting Coronary Stent North American Trial

Prior treatment

• Subject has a known allergy to contrast (that cannot be adequately pre-medicated) and/or the trial stent system or any protocol-required concomitant medications or devices (e.g. cobalt chromium alloy, stainless steel, sirolimus, everolimus or structurally related compounds, polymer, any P2Y12 inhibitor, or aspirin).
• Planned surgery within 6 months.
• Participation in another investigational drug or device trial that has not yet reached its primary endpoint and that may interfere with protocol compliance or confound data interpretation (as per the opinion of the investigator); or intent to participate in another investigational drug or device trial within 12 months.
• Pregnancy or nursing (women of child-bearing potential must have a pregnancy test within 7 days prior to the index procedure).
• Subject has received an organ transplant or is on a waiting list for an organ transplant.
• Subject is receiving oral or intravenous immunosuppressive therapy or has known life-limiting immunosuppressive or autoimmune disease (e.g., HIV). Corticosteroids are allowed.
  • Angiographic Exclusion Criteria:
• Prior PCI in the target vessel in the 12 months prior to enrollment

Other illness

• History of stent thrombosis.
• Clinically significant liver disease.
• Active peptic ulcer or active bleeding from any site.
• Other serious medical illness with a life-expectancy \< 24 months (e.g. cancer, severe heart failure, severe lung disease).
• Any co-morbid condition that may cause non-compliance with the protocol (e.g. dementia, substance abuse, etc.).

Lab values

• Known LVEF \<30%.
• Calculated creatinine clearance \<30 mL/min using Cockcroft-Gault equation (\<40 mL/min for subjects participating in the angiographic follow-up sub-study).
• Hemoglobin \<10 g/dL.
• Platelet count \<100,000 cells/mm3 or \>700,000 cells/mm3.
• White blood cell (WBC) count \<3,000 cells/mm3.

Other

• STEMI within 24 hours of initial time of presentation to the first treating hospital, whether at a transfer facility or the study hospital or in whom enzyme levels (either CK-MB or Troponin) have not peaked.
• PCI within the 24 hours preceding the baseline procedure.
• Cardiogenic shock (defined as persistent hypotension (systolic blood pressure \<90 mm/Hg for more than 30 minutes) or requiring pressors or hemodynamic support, including IABP.
• Subject is intubated.
• Subject has an indication for chronic oral anticoagulant treatment (with either vitamin K antagonists or novel anticoagulants - NOACs)
• A planned procedure that may cause non-compliance with the protocol or confound data interpretation.
• Intention to become pregnant within 12 months (women of child-bearing potential who are sexually active must agree to use contraceptives from the time of enrollment through 12 months post-procedure).
• Unprotected left main interventions
• Bifurcation lesions with intended dual stent implantations
• DES restenotic lesions
• Any lesion in the target vessel that is likely to require PCI within 12 months
• Stent lengths \>36mm for diameters 2.0 mm and 2.25 mm (i.e., very long thin stents).
• Lesion with intended ≥ 3 stent implantation

• Age ≥ 18 years.
• Patient understands the trial requirements and treatment procedures and provides written informed consent prior to any trial-specific tests or treatment.
• Patients with an indication for PCI including angina (stable or unstable), silent ischemia (in absence of symptoms a visually estimated target lesion diameter stenosis of ≥70%, a positive non-invasive stress test, or a positive coronary physiology test (e.g. FFR≤0.80 or iFR\<0.90 or rFR ≤ 0.89 must be present), NSTEMI, or recent STEMI (STEMI \>24 hours and in whom enzyme levels have peaked). For STEMI the time of presentation to the first treating hospital, whether a transfer facility or the study hospital, must be \>24 hours prior to randomization and enzyme levels (CK-MB or Troponin) demonstrating that either or both enzyme levels have peaked.
• Patient is willing to comply with all protocol-required follow-up evaluations.
  • Angiographic inclusion criteria:
• Target lesion(s) must be located in a native coronary artery with visually estimated diameter of ≥2.25 mm to ≤4.0 mm and up to 44 mm in length.
• The coronary anatomy is deemed likely to allow delivery of a study device to the target lesion(s).
• Complex lesions are allowed including calcified lesions (lesion preparation is allowed and strongly recommended with current approved devices (e.g. scoring/cutting balloon and rotational/orbital atherectomy), multivessel disease, CTO,bifurcation lesions (except planned dual stent implantation), ostial lesions, tortuous lesions, and protected left main lesions.
• Overlapping stents are allowed