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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.

Publication ,  Journal Article
Kong, DF; Saito, S; Nakamura, S; Mehran, R; Rowland, SM; Handler, A; Al-Khalidi, HR; Krucoff, MW
Published in: Am Heart J
May 2017

Tissue trauma associated with stent implantation continues to generate early thrombosis rates of 0.9% to 1.3% for both bare-metal and drug-eluting stent platforms. The Combo sirolimus-eluting stent combines an abluminal, bioabsorbable polymer with a luminal CD34+ antibody designed to capture endothelial progenitor cells. This article describes the design and methods of the HARMONEE trial (NCT02073565), which represents the first randomized controlled trial of the Combo design against a best-in-class contemporary everolimus-eluting stent. Up to 50 sites in Japan and the United States will enroll 286 subjects (271 evaluable) in each of 2 arms, for a total sample size of 572 subjects (542 evaluable). The statistical plan includes both superiority to imputed bare-metal stent control and noninferiority to everolimus-eluting stent on a primary clinical end point of target vessel failure at 1 year. In addition, fractional flow reserve assessment to evaluate the physiology of target vessels in the entire population will augment the end point definition of ischemia-driven target vessel revascularization. Finally, key safety considerations will be evaluated with a subpopulation with optical coherence tomography imaging for strut coverage, late strut malapposition, and plaque volume, as well as serial human antimurine antibody assessments. As the first international prospective randomized coronary intervention study under the "Harmonization by Doing" program, this study represents a unique collaboration between regulators and investigators in Japan and the United States.

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Published In

Am Heart J

DOI

EISSN

1097-6744

Publication Date

May 2017

Volume

187

Start / End Page

112 / 121

Location

United States

Related Subject Headings

  • Tomography, Optical Coherence
  • Single-Blind Method
  • Research Design
  • Purinergic P2Y Receptor Antagonists
  • Prosthesis Design
  • Polymers
  • Myocardial Ischemia
  • Humans
  • Drug-Eluting Stents
  • Cardiovascular System & Hematology
 

Citation

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Kong, David F., Shigeru Saito, Shigeru Nakamura, Roxana Mehran, Stephen M. Rowland, Allison Handler, Hussein R. Al-Khalidi, and Mitchell W. Krucoff. “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 187 (May 2017): 112–21. https://doi.org/10.1016/j.ahj.2017.02.004.
Journal cover image

Published In

Am Heart J

DOI

EISSN

1097-6744

Publication Date

May 2017

Volume

187

Start / End Page

112 / 121

Location

United States

Related Subject Headings

  • Tomography, Optical Coherence
  • Single-Blind Method
  • Research Design
  • Purinergic P2Y Receptor Antagonists
  • Prosthesis Design
  • Polymers
  • Myocardial Ischemia
  • Humans
  • Drug-Eluting Stents
  • Cardiovascular System & Hematology