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A Phase 2, randomized, partially blinded, active-controlled study assessing the efficacy and safety of variable anticoagulation reversal using the REG1 system in patients with acute coronary syndromes: results of the RADAR trial

Authors :
Thomas J, Povsic
John P, Vavalle
Laura H, Aberle
Jaroslaw D, Kasprzak
Mauricio G, Cohen
Roxana, Mehran
Christoph, Bode
Christopher E, Buller
Gilles, Montalescot
Jan H, Cornel
Andrzej, Rynkiewicz
Michael E, Ring
Uwe, Zeymer
Madhu, Natarajan
Nicolas, Delarche
Steven L, Zelenkofske
Richard C, Becker
John H, Alexander
Rebecca, Torguson
Source :
European Heart Journal. 34:2481-2489
Publication Year :
2012
Publisher :
Oxford University Press (OUP), 2012.

Abstract

Aims We sought to determine the degree of anticoagulation reversal required to mitigate bleeding, and assess the feasibility of using pegnivacogin to prevent ischaemic events in acute coronary syndrome (ACS) patients managed with an early invasive approach. REG1 consists of pegnivacogin, an RNA aptamer selective factor IXa inhibitor, and its complementary controlling agent, anivamersen. REG1 has not been studied in invasively managed patients with ACS nor has an optimal level of reversal allowing safe sheath removal been defined. Methods and results Non-ST-elevation ACS patients ( n = 640) with planned early cardiac catheterization via femoral access were randomized 2:1:1:2:2 to pegnivacogin with 25, 50, 75, or 100% anivamersen reversal or heparin. The primary endpoint was total ACUITY bleeding through 30 days. Secondary endpoints included major bleeding and the composite of death, myocardial infarction, urgent target vessel revascularization, or recurrent ischaemia. Enrolment in the 25% reversal arm was suspended after 41 patients. Enrolment was stopped after three patients experienced allergic-like reactions. Bleeding occurred in 65, 34, 35, 30, and 31% of REG1 patients with 25, 50, 75, and 100% reversal and heparin. Major bleeding occurred in 20, 11, 8, 7, and 10% of patients. Ischaemic events occurred in 3.0 and 5.7% of REG1 and heparin patients, respectively. Conclusion At least 50% reversal is required to allow safe sheath removal after cardiac catheterization. REG1 appears a safe strategy to anticoagulate ACS patients managed invasively and warrants further investigation in adequately powered clinical trials of patients who require short-term high-intensity anticoagulation. Clinical Trials Registration: ClinicalTrials.gov [NCT00932100][1]. [1]: /lookup/external-ref?link_type=CLINTRIALGOV&access_num=NCT00932100&atom=%2Fehj%2Fearly%2F2012%2F08%2F01%2Feurheartj.ehs232.atom

Details

ISSN :
15229645 and 0195668X
Volume :
34
Database :
OpenAIRE
Journal :
European Heart Journal
Accession number :
edsair.doi.dedup.....71926e60282262535c515e873ce2170b
Full Text :
https://doi.org/10.1093/eurheartj/ehs232