Zalunfiban at First Medical Contact for ST-Elevation Myocardial Infarction

In patients with STEMI, zalunfiban administered at first medical contact significantly improved preintervention infarct-related patency and reduced the likelihood of a worse 30-day multicomponent hierarchical clinical end point. Zalunfiban was not associated with increased severe or life-threatening bleeding but was associated with increased mild to moderate bleeding. (Funded by CeleCor Therapeutics; CELEBRATE ClinicalTrials.gov number, NCT04825743.).

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Publication Details

Journal
NEJM Evidence
Published
2025-11-10
DOI
https://doi.org/10.1056/evidoa2500268
Citations
7
Primary Topic
Acute Myocardial Infarction Research
Type
article
Field-Weighted Citation Impact
9.72
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article

Zalunfiban at First Medical Contact for ST-Elevation Myocardial Infarction

Tim P. van de Hoef, G Montalescot, Ellis F. Unger, Robert C. Welsh et al.
7 citations
NEJM Evidence
Acute Myocardial Infarction Research
9.72
article

Zalunfiban at First Medical Contact for ST-Elevation Myocardial Infarction

Tim P. van de Hoef, G Montalescot, Ellis F. Unger, Robert C. Welsh, J. Wouter Jukema, Karin Arkenbout, Henri van de Wetering, Fatih Arslan, Patrick Ecollan, Dragoş Vinereanu, Michael Magro, Rudolf T Tolsma, Rick van der Vliet, Janet Wittes, Renicus S. Hermanides, Gert K. van Houwelingen, René Boomars, Daniel Cociorva, Marcel E. Durieux, Barry S. Coller, Lex A. W. Ruiters, Robert P. Giugliano, M. Gosselink, Frédéric Lapostolle, Valentin Chioncel, Petr Kala, Ron Pisters, Saman Rasoul, Jawed Polad, Janne Beelen, Ashley Verburg, Wouter Remkes, Jindra Vainer, Béla Péter Merkely, Miles Levy, Arnoud W.J. van ‘t Hof, G. Hengstman, Alexandra Arias‐Mendoza, S. A. O. F. Rikken, J. M. ten Berg, A van Beurden, C. B. Granger, James L. Januzzi, N. Baron, C. Michael Gibson, Ben J L Van den Branden
article en
7 citations

Abstract

In patients with STEMI, zalunfiban administered at first medical contact significantly improved preintervention infarct-related patency and reduced the likelihood of a worse 30-day multicomponent hierarchical clinical end point. Zalunfiban was not associated with increased severe or life-threatening bleeding but was associated with increased mild to moderate bleeding. (Funded by CeleCor Therapeutics; CELEBRATE ClinicalTrials.gov number, NCT04825743.).

NEJM EvidenceVol. 5(1)
Semmelweis University (HU), Brigham and Women's Hospital (US), AARP (US), Harvard University (US), University of Alberta (CA), Carol Davila University of Medicine and Pharmacy (RO), Duke University (US), Masaryk University (CZ), Leiden University Medical Center (NL), Medisch Spectrum Twente (NL), Alaska Native Medical Center (US), University Medical Center Utrecht (NL), Maastricht University (NL), Sorbonne Université (FR), Massachusetts General Hospital (US), Ambulance Care (Sweden) (SE), University Hospital Brno (CZ), St. Antonius Ziekenhuis (NL), Netherlands Heart Institute (NL), Amphia Ziekenhuis (NL), Canadian VIGOUR Centre (CA), Baim Institute for Clinical Research (US), VieCuri Medisch Centrum (NL), Pitié-Salpêtrière Hospital (FR), RED Consulting (Norway) (NO), Hôpital Avicenne (FR), Zuyderland Medisch Centrum (NL), Isala (NL), Tergooi (NL), Elisabeth-TweeSteden Ziekenhuis (NL), Rijnstate Hospital (NL), GGZ Oost Brabant (NL), Instituto Nacional de Cardiología (MX), Thrombolysis in Myocardial Infarction Study Group (US), Jeroen Bosch Ziekenhuis (NL), Rockefeller University (US)
Openalex Percentile: Top 2%
Acute Myocardial Infarction Research
9.72
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