Advanced NanoTherapies Dual-API DCB to Treat De-Novo and ISR Lesions in Patients With Symptomatic Coronary Artery Disease (ADVANCE-DUO)

Advanced NanoTherapies

Status: Enrolling

Conditions: NSTEMI - Non-ST Segment Elevation MI; Unstable Angina; Angina (Stable); CAD - Coronary Artery Disease

Treatments: Device: SirPlux Duo™ Dual API-Coated PTCA Balloon Catheter

Study type: Interventional

Funder types: Industry

Identifiers

NCT07368933

ANT-00001

Details and patient eligibility

About

The study objectives are:

1. To evaluate the safety and performance of the SirPlux Duo PTCA to treat coronary ISR lesions 2.00-4.00 mm (inclusive) in diameter in patients with symptomatic coronary artery disease.
2. To evaluate the safety and performance of the SirPlux Duo PTCA to treat coronary de novo lesions <3.00 mm in diameter in patients with symptomatic coronary artery disease.

Enrollment: 30 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. ≥18 years or minimum legal age as required by local regulations.

2. Documented stable or unstable angina, positive functional test, or non -ST elevation myocardial infarction which, in the judgment of the operator, is attributable to disease in coronary vessel or in-stent restenosis, and the patient is deemed an appropriate candidate for PCI in accordance with the applicable guidelines on percutaneous coronary intervention.

   Note: participants with NSTEMI must have enzymes that are trending down or are within normal limits prior to enrollment.

3. Life expectancy >1 year in the Investigator's opinion.

4. Participant is willing and able to cooperate with study procedures and follow-up evaluations.

5. Treatment of only one target lesion required

   1. Tandem lesions treated by a single DCB will be considered one target lesion.
   2. Up to one de novo lesion in a separate vessel may be treated per standard of care at the procedure. Non-target lesions must be successfully treated under the same criteria of the target lesion, before treating the target lesion.

6. Target lesion must be ≤36 mm in length.

7. Target lesion must have a stenosis ≥ 50% and < 100%.

8. Target lesion must have a visually estimated reference vessel diameter of:

   1. ISR lesions: 2.0 to 4.0 mm in diameter (inclusive)
   2. de novo lesions: 2.0 to <3.0 mm in diameter

9. ISR lesions only: target lesion must be within a previous BMS or DES that does not extend >5.0 mm beyond the proximal or distal edge.

Exclusion criteria

1. Participant is pregnant, or breastfeeding. Note: Participant of childbearing potential must have a negative pregnancy test within 7 days before procedure.

2. Known hypersensitivity or contraindication to antiplatelet medications (e.g., aspirin; heparin; prasugrel); or a sensitivity to contrast media which cannot be adequately pre-medicated.

3. History of an allergic reaction or significant sensitivity to paclitaxel, sirolimus, or any other analogue or derivative.

4. Platelet count < 100,000 cells/mm³ (i.e., 100 x 109 /L) or > 700,000 cells/mm³ (i.e., 700 x 10 9 /L), or a white blood cell (WBC) count < 3,000 cells/mm³ within 7 days prior to procedure.

5. Renal insufficiency (Serum creatinine level > 2.5 mg/dl (i.e., 221 μmol/L) within 7 days prior to procedure) or failure (dialysis dependent).

6. Evidence of an acute MI within 72 hours of the procedure Note: participants with NSTEMI are allowed, provided enzymes are trending down or are within normal limits prior to enrollment.

7. Previous PCI of the target vessel within 6 months prior to procedure.

8. History of a stroke or transient ischemic attack (TIA) within the prior 3 months to procedure (any prior stroke or TIA, if prasugrel is used).

9. Planned PCI of any vessel within 30 days post-procedure and/or planned PCI of the target vessel within 12 months post-procedure.

10. Active peptic ulcer or upper gastrointestinal (GI) bleeding within the prior 6 months to procedure.

11. History of bleeding diathesis or coagulopathy or will refuse blood transfusions.

12. Documented left ventricular ejection fraction (LVEF) <30% at the most recent evaluation, within the prior 3 months to procedure.

13. Planned surgery that would cause interruption in recommended DAPT duration per current guidelines.

14. Currently participating in an investigational drug or another device study that has not completed the primary endpoint or that clinically interferes with the current study endpoints; or requires additional coronary angiography, IVUS, or other coronary artery imaging procedures.

15. The following criteria related to previous treatments applies based on the type of lesion treated. The participant is excluded in the following circumstances:

    1. ISR lesions: If single-layer ISR, any previous treatment of the target vessel for restenosis. If double- layer ISR, any treatment of the double-layer ISR.
    2. de novo lesions: any previous treatment of the target lesion.

16. Planned PCI of three vessel disease during procedure.

17. Planned treatment of more than one target vessel. Tandem lesions that can be treated by a single DCB are permissible.

18. Target lesion requires treatment with atherectomy, laser, or thrombectomy procedure.

19. Target vessel has other lesions with greater than 50% diameter stenosis based on visual estimate.

20. Target vessel has evidence of thrombus.

21. Target vessel is excessively tortuous, defined as more than one bend >90° to reach target lesion.

22. Target lesion has any of following characteristics:

    1. Lesion location is unprotected in left main coronary artery, internal mammary artery, aorto-ostial, bypass grafts, ostial lesions or within 5 mm of the origin of the left anterior descending or left circumflex.
    2. Involves a side branch >2.0 mm in diameter.
    3. Is severely calcified.

23. The following criteria based on number and type of lesions:

    1. ISR and de novo lesions: target lesion is in the same vessel with a de novo lesion requiring treatment.
    2. ISR lesions: planned treatment of a ≥3 layer ISR lesion.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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30 participants in 1 patient group

SirPlux Duo™ Dual API-Coated PTCA Balloon Catheter

Experimental group

Description:

Subject who meet the inclusion criteria and agree to participate in the study will be enrolled and undergo a planned percutaneous coronary intervention with SirPlux DUO PTCA

Treatment:

Device: SirPlux Duo™ Dual API-Coated PTCA Balloon Catheter