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The CSL112-2001 trial: Safety and tolerability of multiple doses of CSL112 (apolipoprotein A-I [human]), an intravenous formulation of plasma-derived apolipoprotein A-I, among subjects with moderate renal impairment after acute myocardial infarction.

Authors :
Gibson, C. Michael
Kerneis, Mathieu
Yee, Megan K.
Daaboul, Yazan
Korjian, Serge
Mehr, Ali Poyan
Tricoci, Pierluigi
Alexander, John H.
Kastelein, John J.P.
Mehran, Roxana
Bode, Christoph
Lewis, Basil S.
Mehta, Ravindra
Duffy, Danielle
Feaster, John
Halabi, Majdi
Angiolillo, Dominick J.
Duerschmied, Daniel
Ophuis, Ton Oude
Merkely, Bela
Source :
American Heart Journal; Feb2019, Vol. 208, p81-90, 10p
Publication Year :
2019

Abstract

<bold>Background: </bold>CSL112 (apolipoprotein A-I [human]) is a plasma-derived apolipoprotein A-I developed for early reduction of cardiovascular risk following an acute myocardial infarction (AMI). The safety of CSL112 among AMI subjects with moderate, stage 3 chronic kidney disease (CKD) is unknown.<bold>Methods: </bold>CSL112_2001, a multicenter, placebo-controlled, parallel-group, double-blind, randomized phase 2 trial, enrolled patients with moderate CKD within 7 days following AMI. Enrollment was stratified on the basis of estimated glomerular filtration rate and presence of diabetes requiring treatment. Patients were randomized in a 2:1 ratio to receive 4 weekly infusions of CSL112 6 g or placebo. The co-primary safety end points were renal serious adverse events (SAEs) and acute kidney injury, defined as an increase ≥26.5 μmol/L in baseline serum creatinine for more than 24 hours, during the treatment period.<bold>Results: </bold>A total of 83 patients were randomized (55 CSL112 vs 28 placebo). No increase in renal SAEs was observed in the CSL112 group compared with placebo (CSL112 = 1 [1.9%], placebo = 4 [14.3%]). Similarly, no increase in acute kidney injury events was observed (CSL112 = 2 [4.0%], placebo = 4 [14.3%]). Rates of other SAEs were similar between groups. CSL112 administration resulted in increases in ApoA-I and cholesterol efflux similar to those observed in patients with AMI and normal renal function or stage 2 CKD enrolled in the ApoA-I Event Reducing in Ischemic Syndromes I trial.<bold>Conclusions: </bold>These results demonstrate the acceptable safety of the 6-g dose of CSL112 among AMI subjects with moderate stage 3 CKD and support inclusion of these patients in a phase 3 cardiovascular outcomes trial powered to assess efficacy. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00028703
Volume :
208
Database :
Supplemental Index
Journal :
American Heart Journal
Publication Type :
Academic Journal
Accession number :
134795922
Full Text :
https://doi.org/10.1016/j.ahj.2018.11.008