casirivimab/imdevimab (REGEN-COV)在COVID-19妊娠个体中的有效性和安全性:文献综述和来自COVID-19国际药物妊娠登记处的见解

IF 0.8 Q4 OBSTETRICS & GYNECOLOGY
Diego F Wyszynski, Vincent Yau, Daniel Keebler, Cheryl Renz, Jane Ives, Andrew Fitzgibbon, Lee P Shulman
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引用次数: 0

摘要

Casirivimab/imdevimab (CAS/IMD)由两种单克隆抗体组成,可中和SARS-CoV-2。孕妇被排除在初始试验之外,限制了安全性数据。方法:在COVID-19国际药物妊娠登记处登记了53例接受CAS/IMD治疗的孕妇,其中34例活产。结果:未发现安全问题。讨论和结论:COVID-PR研究的结果支持妊娠期间CAS/IMD的安全性,为这一人群的COVID-19治疗提供了越来越多的证据。现有文献表明,CAS/IMD可有效预防孕妇发展为严重的COVID-19。这些药物耐受性良好,没有令人信服的证据表明有不良的孕产妇或新生儿结局。COVID-PR研究的结果与更广泛的文献一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and safety of casirivimab/imdevimab (REGEN-COV) in pregnant individuals with COVID-19: Literature review and insights from the COVID-19 International Drug Pregnancy Registry.

Introduction: Casirivimab/imdevimab (CAS/IMD) comprises two monoclonal antibodies that neutralize SARS-CoV-2. Pregnant individuals were excluded from initial trials, limiting safety data.

Methods: The COVID-19 International Drug Pregnancy Registry enrolled 53 pregnant women treated with CAS/IMD, with 34 live births.

Results: No safety concerns were identified.

Discussion and conclusions: The findings of the COVID-PR study support the safety of CAS/IMD during pregnancy, adding to the growing body of evidence on COVID-19 treatments for this population. The available literature shows that CAS/IMD is effective in preventing the progression to severe COVID-19 in pregnant individuals. The drugs are well-tolerated, and there is no compelling evidence of adverse maternal or neonatal outcomes. The results from the COVID-PR study are consistent with those of the broader literature.

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来源期刊
Obstetric Medicine
Obstetric Medicine OBSTETRICS & GYNECOLOGY-
CiteScore
1.90
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0.00%
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60
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