Design of a phase 2b trial of intracoronary administration of AAV1/SERCA2a in patients with advanced heart failure: the CUPID 2 trial (calcium up-regulation by percutaneous administration of gene therapy in cardiac disease phase 2b).

Barry Greenberg, Alex Yaroshinsky, Krisztina M Zsebo, Javed Butler, G Michael Felker, Adriaan A Voors, Jeffrey J Rudy, Kim Wagner, Roger J Hajjar

Journal: JACC. Heart failure 2015;2(1):84-92

PMID: 24622121

Abstract

OBJECTIVES

Impaired cardiac isoform of sarco(endo)plasmic reticulum Ca(2+) ATPase (SERCA2a) activity is a key abnormality in heart failure patients with reduced ejection fraction. The CUPID 2 (Calcium Up-Regulation by Percutaneous Administration of Gene Therapy in Cardiac Disease Phase 2b) trial is designed to evaluate whether increasing SERCA2a activity via gene therapy improves clinical outcome in these patients.

BACKGROUND

Intracoronary delivery of recombinant adeno-associated virus serotype 1 (AAV1)/SERCA2a improves intracellular Ca(2+) handling by increasing SERCA2a protein levels and, as a consequence, restores systolic and diastolic function. In a previous phase 2a trial, this therapy improved symptoms, functional status, biomarkers, and left ventricular function, and reduced cardiovascular events in advanced heart failure patients.

METHODS

CUPID 2 is a phase 2b, double-blind, placebo-controlled, multinational, multicenter, randomized event-driven study in up to 250 patients with moderate-to-severe heart failure with reduced ejection fraction and New York Heart Association functional class II to IV symptoms despite optimal therapy. Enrolled patients will be at high risk for recurrent heart-failure hospitalizations by virtue of having elevated N-terminal pro-B-type natriuretic peptide/BNP (>1,200 pg/ml, or >1,600 pg/ml if atrial fibrillation is present) and/or recent heart failure hospitalization. The primary endpoint of time-to-recurrent event (heart failure-related hospitalizations in the presence of terminal events [all-cause death, heart transplant, left ventricular assist device implantation or ambulatory worsening heart failure]) will be assessed using the joint frailty model. This ongoing trial is expected to complete recruitment in 2014, with the required number of 186 recurrent events estimated to occur by mid 2015.

RESULTS

Available data indicate that calcium up-regulation by AAV1/SERCA2a gene therapy is safe and of potential benefit in advanced heart failure patients.

CONCLUSIONS

The CUPID 2 trial is designed to study the effects of this therapy on clinical outcome in these patients. (Calcium Up-Regulation by Percutaneous Administration of Gene Therapy in Cardiac Disease Phase 2b [CUPID-2b]; NCT01643330).

Copyright © 2014 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Address: Division of Cardiovascular Medicine, University of California at San Diego, San Diego, California. Electronic address: [email protected].; AY Statistical Consulting, San Andreas, California.; Celladon Corporation, San Diego, California.; Emory Clinical Cardiovascular Research Institute, Atlanta, Georgia.; Division of Cardiology, Duke University School of Medicine, Durham, North Carolina.; Department of Cardiology, University Medical Center Groningen, Groningen, the Netherlands.; Cardiovascular Research Center, Icahn School of Medicine at Mount Sinai School of Medicine, New York, New York.
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