HARMONEE - Japan-USA Harmonized Assessment by Randomized, Multi-Center Study of OrbusNEich's Combo StEnt

NCT ID: NCT02073565

Last Updated: 2022-05-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 572 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-02-28
• Study Completion Date: 2021-12-31

Brief Summary

This is a multi-center, single-blind, randomized, active-controlled, clinical trial in Percutaneous Coronary Intervention (PCI) subjects. Subjects will be randomized to receive the Combo stent as the investigational treatment arm or an Everolimus Eluting Stent (EES) as the active-control arm.

Detailed Description

Up to 50 sites are proposed in Japan and the United States to enroll 286 subjects (271 evaluable) in each of 2 arms, for a total sample size of 572 subjects (542 evaluable) who are admitted to the hospital for a planned (elective and urgent) percutaneous coronary artery intervention procedure.

After stent implantation, subjects will be contacted for follow-up at 30 days; 6 months; and 1, 2, 3, 4, and 5 years. At 12 months a clinical evaluation will be completed before cardiac catheterization and angiographic assessment.

Rationale: This study is intended to demonstrate that the Combo stent platform shows superiority to an imputed Bare Metal Stent (BMS) performance goal, noninferior effectiveness and safety vs best-in-class second-generation everolimus-eluting stent (EES) (Xience V, Xience Prime, Xience Xpedition stents; [Abbott Vascular/Abbott Vascular Japan]), and evidence of mechanistic activity of the anti-CD34-Ab endothelial progenitor cell (EPC) capture technology with healthy level of intimal tissue coverage superior to that of the best-in-class EES.

To ensure the robustness and interpretability of results, the current proposal includes a number of unique design features:

• Largest randomized Drug-Eluting Stent (DES) study ever performed in Japan
• Enriched population, including stabilized Non-ST-elevation myocardial infarction (NSTEMI) subjects with greater likelihood of plaque rupture associated with their clinical syndromes
• Collaboration between with Japan and the United States as a "Proof of Concept" program under the auspices of the Harmonization by Doing Initiative, Working Group 1 (WG 1), including concomitant enrollment in U.S.A. sites as an FDA-approved Investigational Device Exemption (IDE) study
• Head-to-head randomization against state-of-the-art EES platform control, analyzed for clinical noninferiority
• Statistical analysis vs imputed BMS analyzed for clinical superiority
• Fractional flow reserve (FFR) follow-up of 100% of subjects enrolled, providing clinically relevant physiologic assessment of all subjects for 1 year ischemia-driven Target Vessel Revascularization (TVR) analysis
• Mechanistic Optical coherence tomography (OCT) imaging observations in 140 subjects using 6 French catheters as follows:

• Cohort A (30 subjects, 1:1 Combo and EES): Mechanistic imaging observations to provide serial 6 month and 1 year OCT evaluation of healthy intimal tissue coverage, intracoronary thrombosis, and stent malapposition and quantitative coronary angiographic (QCA) analysis to assess 1 year late loss.
• Cohort B (110 subjects, 1:1 Combo and EES): Mechanistic imaging observations to assess 1 year OCT evaluation of healthy intimal tissue coverage, intracoronary thrombosis, and stent malapposition, and QCA analysis to assess 1 year late loss. Combined with the 12 month imaging of Cohort A, this study will provide OCT and QCA observations at 1 year in 140 patients, half with Combo and half with EES.
• Cohort C: 432 subjects (216 subjects per arm) will undergo all clinical follow-up assessments with FFR and angiographic assessments at 12 months. Cohort C will be the last cohort to enroll.
• In the 110 subjects in Cohort B, 30 day and 1 year human antimurine antibody (HAMA) titers will also be collected.

Conditions

Coronary Arteriosclerosis; Non ST Segment Elevation Acute Coronary Syndrome

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Combo

The Combo Stent is composed of the OrbusNeich R stent™, with an abluminal coating of a bioabsorbable polymer matrix formulated with sirolimus for sustained release, and an anti-CD34 antibody cell capture coating on the luminal surface.

Group Type: EXPERIMENTAL

OrbusNeich Combo stent™

Intervention Type: DEVICE

The Combo Stent is composed of the OrbusNeich R stent™, with an abluminal coating of a bioabsorbable polymer matrix formulated with sirolimus for sustained release, and an anti-CD34 antibody cell capture coating on the luminal surface.

Everolimus Eluting Stent (EES)

Everolimus Eluting Stent (EES) (Xience V, Xience Prime, Xience Xpedition stents, Abbott Vascular/Abbott Vascular Japan). Xience Prime inherited the clinical result of Xience V and is a product that obtains efficiency essentially equal to Xience V.

Group Type: ACTIVE_COMPARATOR

Everolimus Eluting Stent (EES)

Intervention Type: DEVICE

Everolimus Eluting Stent (EES) (Xience V, Xience Prime, Xience Xpedition stents, Abbott Vascular/Abbott Vascular Japan). Xience Prime inherited the clinical result of Xience V and is a product that obtains efficiency essentially equal to Xience V.

Interventions

OrbusNeich Combo stent™

The Combo Stent is composed of the OrbusNeich R stent™, with an abluminal coating of a bioabsorbable polymer matrix formulated with sirolimus for sustained release, and an anti-CD34 antibody cell capture coating on the luminal surface.

Intervention Type: DEVICE

Everolimus Eluting Stent (EES)

Everolimus Eluting Stent (EES) (Xience V, Xience Prime, Xience Xpedition stents, Abbott Vascular/Abbott Vascular Japan). Xience Prime inherited the clinical result of Xience V and is a product that obtains efficiency essentially equal to Xience V.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

To be eligible for this trial, subjects must meet all of the following criteria:

1. Subject is able to verbally confirm understanding of risks, benefits, and treatment alternatives of Combo vs EES stent, and the subject or a legally authorized representative (LAR) must provide written informed consent before any study-related procedures are performed.

2. Subject must be at least 20 years of age at the time of randomization.

3. Subject must have clinical or functional evidence of myocardial ischemia (eg, stable or unstable angina, stabilized non-ST-elevation myocardial infarction confirmed by serum markers, ischemia by positive functional study, abnormal FFR, or a reversible change in the electrocardiogram (ECG) consistent with ischemia).

4. Subject must be acceptable candidate with anatomy suitable for PCI with a DES.

5. Subject agrees to return for all study-related follow-up assessments, including invasive OCT follow-up assessment at 6 months (Cohort A) and at 1 year postprocedure (Cohorts A, B, and C).

6. Subject is an acceptable candidate for Coronary artery bypass grafting (CABG) surgery.

Angiographic Anatomy Criteria-

7. Target lesions must be located in a native coronary artery with visually estimated diameter of 2.5 mm to 3.5 mm, inclusive, and up to 3 de novo target lesions may be treated, with a maximum of 2 de novo target lesions per epicardial vessel, with a maximum of 2 target vessels.

8. Target lesions should be treatable with a single stent, and must measure 28 mm or less in length by visual estimation (2 mm or more of nondiseased tissue on either side of the target lesion should be covered by the study stent).

9. If more than 1 target lesion will be treated, the reference vessel diameter and lesion length of each target lesion must meet the above criteria.

10. Target lesions must be in a major artery or branch with a visually estimated stenosis of 50% or greater and less than 100% with a Thrombolysis in Myocardial Infarction (TIMI) flow of 1 or greater.

11. Previous percutaneous intervention of lesions in a target vessel (including side branches) is allowed if done 9 or more months before the study procedure and greater than 10 mm from the current target lesion.

12. Nonstudy percutaneous interventions for lesions in a nontarget vessel are allowed if done 9 or more months before the study procedure, in the absence of documented ischemia or angiographic restenosis related to the vessel.

Exclusion Criteria

If a subject meets any of the following criteria, he or she may not be enrolled in the study:

1. ST-Elevation Myocardial Infarction (STEMI) at index presentation or within 7 days of study screening.

2. Subject has current unstable arrhythmias or intractable angina with ECG changes or shock requiring pressors or mechanical assist device (intraaortic balloon pump, left ventricular assist device, Impella, etc.).

3. Subject has known left ventricular ejection fraction (LVEF) less than 30%.

4. Subject has received a heart transplant or any other organ transplant or is on a waiting list for any organ transplant.

5. Subject is receiving or scheduled to receive anticancer therapy for malignancy within 30 days before or after the procedure.

6. Subject is receiving immunosuppression therapy, has known serious immunosuppressive disease (eg, human immunodeficiency virus), or has severe autoimmune disease that requires chronic immunosuppressive therapy (eg, systemic lupus erythematosus).

7. Subject has known hypersensitivity or contraindication to aspirin; both heparin and bivalirudin; all available P2Y12 inhibitors (clopidogrel, prasugrel, ticlopidine, and ticagrelor); any everolimus, sirolimus, cobalt, chromium, nickel, tungsten, acrylic, or fluoro polymers; or hypersensitivity to contrast media that cannot be adequately premedicated.

8. Subject has previously received murine therapeutic antibodies and exhibited sensitization through the production of human anti-mouse antibodies (HAMAs).

9. Subject has elective surgery planned within the first 12 months after the procedure that will require interruption or discontinuation of planned Dual Antiplatelet Therapy (DAPT).

10. Subject has known platelet count less than 100,000 cells/mm3 or greater than 700,000 cells/mm3, a white blood cell count of less than 3000 cells/mm3, or documented or suspected liver disease (including laboratory evidence of hepatitis).

11. Subject has known renal insufficiency (eg, serum creatinine level of greater than 2.5 mg/dL or subject is on dialysis).

12. Subject has history of bleeding diathesis or coagulopathy or will refuse blood transfusions.

13. Subject has had a cerebrovascular accident or transient ischemic neurological attack within the past 6 months.

14. Subject has had a significant gastrointestinal or urinary bleed within the past 6 months.

15. Subject has known extensive peripheral vascular disease that precludes safe 6 French sheath insertion.

16. Known other medical illness (eg, cancer, chronic infectious disease, severe vascular disease, or congestive heart failure) or known history of substance abuse (alcohol, cocaine, heroin, etc.) that may cause noncompliance with the protocol, confound the data interpretation, or is associated with a life expectancy of less than 1 year.

17. Currently participating in another clinical study that has not yet reached its primary endpoint.

18. Currently pregnant or breast-feeding or is planning pregnancy in the period up to 1 year following index procedure. Female subjects of childbearing potential must have a negative pregnancy test within 7 days before the index procedure.

If the target lesion meets any of the following criteria, the subject may not be enrolled in the study:

19. Unprotected left main coronary artery location.

20. Unprotected ostial (located within 2 mm of the origin) left anterior descending artery or left circumflex.

21. Located within an arterial or saphenous vein graft or graft anastomosis, distal to a diseased arterial or saphenous vein graft (visually estimated graft diameter stenosis greater than 40%).

22. Involves a bifurcation in which the side branch is 2 mm or greater in diameter AND would be covered by the planned stent.

23. Involves a side branch requiring predilation.

24. Total occlusion (TIMI flow 0) before wire crossing.

25. Extreme tortuosity proximal to or within the lesion.

26. Extreme angulation (90º or greater) proximal to or within the lesion.

27. Heavy calcification, defined as multiple persisting opacifications of the coronary wall visible in more than one projection surrounding the complete lumen of the coronary artery at the site of the lesion.

28. Restenotic vessel from previous intervention.

29. Received brachytherapy in any epicardial vessel (including side branches).

30. Target vessel contains angiographically visible thrombus.

31. Serial lesions or diffuse disease with high probability of bailout requiring 3 or more stents in a single vessel, more than 5 stents per subject, or more than 2 vessels.

32. Target or nontarget vessel lesion (including all side branches) is present with a high probability of requiring PCI within 12 months after the index procedure.

33. Stent overlapping is a planned treatment of the target lesion.

• Minimum Eligible Age: 20 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

OrbusNeich Medical K.K.

UNKNOWN

Sponsor Role: collaborator

Duke Clinical Research Institute

OTHER

Sponsor Role: collaborator

OrbusNeich

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Mitchell W Krucoff, MD

Role: PRINCIPAL_INVESTIGATOR

Duke Clinical Research Institute

Shigeru Saito, MD

Role: PRINCIPAL_INVESTIGATOR

Shonan Kamakura General Hospital

Locations

MedStar Clinical Research Center

Washington D.C., District of Columbia, United States

Atlantic Clinical Research Collaborative-Cardiology

Lake Worth, Florida, United States

University of Miami

Miami, Florida, United States

Tallahassee Research Institute

Tallahassee, Florida, United States

Emory University Hospital Midtown

Atlanta, Georgia, United States

North Georgia Heart Foundation

Gainesville, Georgia, United States

Maine Medical Center

Portland, Maine, United States

Washington Adventist Hospital

Takoma Park, Maryland, United States

Lahey Clinic

Burlington, Massachusetts, United States

North Mississippi Medical Center

Tupelo, Mississippi, United States

Mount Sinai Medical Center

New York, New York, United States

University of Rochester Medical Center-Strong Memorial Hospital

Rochester, New York, United States

Duke University Medical Center

Durham, North Carolina, United States

Wake Forest Baptist Medical Center

Winston-Salem, North Carolina, United States

The Ohio State University Medical Center

Columbus, Ohio, United States

Lehigh Valley Hospital

Allentown, Pennsylvania, United States

Vanderbilt University Medical Center

Nashville, Tennessee, United States

Saiseikai Fukuoka General Hospital

Fukoka-shi, Fukuoka, Japan

Kurume University Hospital

Kurume-shi, Fukuoka, Japan

Shinkoga Hospital

Kurume-shi, Fukuoka, Japan

Tsuchiya General Hospital

Hiroshima, Hiroshima, Japan

Hakodate Municipal Hospital

Hakodate-shi, Hokkaido, Japan

Sapporo Higashi Tokushukai Hospital

Sapporo, Hokkaido, Japan

Hyogo Brain and Heart Centre

Himeji-shi, Hyōgo, Japan

Takahashi Hospital

Kobe, Hyōgo, Japan

Higashi Takarazuka Satoh Hospital

Takarazukasi, Hyōgo, Japan

Tsuchiura Kyodo Hospital

Tsuchiura, Ibaraki, Japan

Kanazawa Cardiovascular Hospital

Kanazawa, Ishikawa-ken, Japan

National Hospital Organisation Kagoshima Medical Centre

Kagoshima, Kagoshima-ken, Japan

Shonan Kamakura General Hospital

Okamoto, Kamakura City, Japan

Kanto Rosai Hospital

Kawasaki-shi, Kanagawa, Japan

Saiseikai Yokohamashi Tobu Hospital

Yokohama, Kanagawa, Japan

Kyoto-Katsura Hospital

Kyoto, Kyoto, Japan

Miyazaki Medical Association Hospital

Miyazaki, Miyazaki, Japan

Kurashiki Central Hospital

Kurashiki-shi, Okayama-ken, Japan

The Sakakibara Heart Institute of Okayama

Okayama, Okayama-ken, Japan

Sakurabashi Watanabe Hospital

Osaka, Osaka, Japan

Osaka Saiseikai Nakatsu Hospital

Osaka, Osaka, Japan

Saga University Hospital

Saga, Saga-ken, Japan

Saitama Prefectural Cardiovascular and Respiratory Disease Centre

Kumagaya-shi, Saitama, Japan

Okamura Memorial Hospital

Suntou-gun, Shizouka, Japan

Jichi Medical University Hospital

Shimotsuke-shi, Tochigi, Japan

Department of Cardiovascular Medicine, Juntendo University School of Medicine

Bunkyo-ku, Tokyo, Japan

Sakakibara Memorial Hospital

Fuchu-shi, Tokyo, Japan

Teikyo University Hospital

Itabashi-ku, Tokyo, Japan

Toho University Ohashi Hospital

Meguro-ku, Tokyo, Japan

The Cardiovascular Institute Hospital

Minato-ku, Tokyo, Japan

Showa University Hospital

Shinagawa-ku, Tokyo, Japan

Cardiac Catheterisation Laboratory, Keio University School of Medicine

Shinjuku-ku, Tokyo, Japan

Tokyo Women's Medical University Hospital

Shinjuku-ku, Tokyo, Japan

Countries

United States; Japan

References

Kong DF, Saito S, Nakamura S, Mehran R, Rowland SM, Handler A, Al-Khalidi HR, Krucoff MW. Rationale and design of the Japan-USA harmonized assessment by randomized, multicenter study of OrbusNEich's combo StEnt (Japan-USA HARMONEE): Assessment of a novel DES platform for percutaneous coronary revascularization in patients with ischemic coronary disease and non-ST-elevation acute coronary syndrome. Am Heart J. 2017 May;187:112-121. doi: 10.1016/j.ahj.2017.02.004. Epub 2017 Feb 12.

Reference Type: BACKGROUND

PMID: 28454795 (View on PubMed)

Saito S, Krucoff MW, Nakamura S, Mehran R, Maehara A, Al-Khalidi HR, Rowland SM, Tasissa G, Morrell D, Joseph D, Okaniwa Y, Shibata Y, Bertolet BD, Rothenberg MD, Genereux P, Bezerra H, Kong DF. Japan-United States of America Harmonized Assessment by Randomized Multicentre Study of OrbusNEich's Combo StEnt (Japan-USA HARMONEE) study: primary results of the pivotal registration study of combined endothelial progenitor cell capture and drug-eluting stent in patients with ischaemic coronary disease and non-ST-elevation acute coronary syndrome. Eur Heart J. 2018 Jul 7;39(26):2460-2468. doi: 10.1093/eurheartj/ehy275.

Reference Type: RESULT

PMID: 29931092 (View on PubMed)

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

OMKK 02

Identifier Type: OTHER

Identifier Source: secondary_id

VP-0601

Identifier Type: -

Identifier Source: org_study_id