Intracoronary delivery of injectable bioabsorbable scaffold (IK-5001) to treat left ventricular remodeling after ST-elevation myocardial infarction: a first-in-man study

Circ Cardiovasc Interv. 2014 Dec;7(6):806-12. doi: 10.1161/CIRCINTERVENTIONS.114.001478. Epub 2014 Oct 28.

Abstract

Background: We aimed to test, for the first time, the feasibility of intracoronary delivery of an innovative, injectable bioabsorbable scaffold (IK-5001), to prevent or reverse adverse left ventricular remodeling and dysfunction in patients after ST-segment-elevation myocardial infarction.

Methods and results: Patients (n=27) with moderate-to-large ST-segment-elevation myocardial infarctions, after successful revascularization, were enrolled. Two milliliters of IK-5001, a solution of 1% sodium alginate plus 0.3% calcium gluconate, was administered by selective injection through the infarct-related coronary artery within 7 days after myocardial infarction. IK-5001 is assumed to permeate the infarcted tissue, cross-linking into a hydrogel and forming a bioabsorbable cardiac scaffold. Coronary angiography, 3 minutes after injection, confirmed that the injection did not impair coronary flow and myocardial perfusion. Furthermore, IK-5001 deployment was not associated with additional myocardial injury or re-elevation of cardiac biomarkers. Clinical assessments, echocardiographic studies, 12-lead electrocardiograms, 24-hour Holter monitoring, blood tests, and completion of Minnesota Living with Heart Failure Questionnaires were repeated during follow-up visits at 30, 90, and 180 days after treatment. During a 6-month follow-up, these tests confirmed favorable tolerability of the procedure, without device-related adverse events, serious arrhythmias, blood test abnormalities, or death. Serial echocardiographic studies showed preservation of left ventricular indices and left ventricular ejection fraction.

Conclusions: This first-in-man pilot study shows that intracoronary deployment of an IK-5001 scaffold is feasible and well tolerated. Our results have promoted the initiation of a multicenter, randomized controlled trial to confirm the safety and efficacy of this new approach in high-risk patients after ST-segment-elevation myocardial infarction.

Clinical trial registration url: http://www.clinicaltrials.gov. Unique identifier: NCT01226563.

Keywords: coronary disease; heart failure; myocardial infarction; ventricular remodeling.

Publication types

  • Clinical Trial
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Absorbable Implants* / adverse effects
  • Adult
  • Aged
  • Alginates / administration & dosage*
  • Alginates / adverse effects
  • Belgium
  • Calcium Gluconate / administration & dosage*
  • Calcium Gluconate / adverse effects
  • Feasibility Studies
  • Female
  • Germany
  • Glucuronic Acid / administration & dosage
  • Glucuronic Acid / adverse effects
  • Heart Function Tests
  • Hexuronic Acids / administration & dosage
  • Hexuronic Acids / adverse effects
  • Humans
  • Hydrogels
  • Injections, Intra-Arterial
  • Male
  • Middle Aged
  • Myocardial Infarction / diagnosis
  • Myocardial Infarction / physiopathology
  • Myocardial Infarction / therapy*
  • Pilot Projects
  • Predictive Value of Tests
  • Regenerative Medicine / methods*
  • Surveys and Questionnaires
  • Time Factors
  • Tissue Engineering / methods*
  • Tissue Scaffolds* / adverse effects
  • Treatment Outcome
  • Ventricular Dysfunction, Left / diagnosis
  • Ventricular Dysfunction, Left / physiopathology
  • Ventricular Dysfunction, Left / therapy*
  • Ventricular Function, Left*
  • Ventricular Remodeling*

Substances

  • Alginates
  • Hexuronic Acids
  • Hydrogels
  • Glucuronic Acid
  • Calcium Gluconate

Associated data

  • ClinicalTrials.gov/NCT01226563