Assessing the safety and pharmacokinetics of casirivimab and imdevimab (CAS+IMD) in a cohort of pregnant outpatients with COVID-19: results from an adaptive, multicentre, randomised, double-blind, phase 1/2/3 study
Authors
John D. Davis (ORCID: https://orcid.org/0000-0001-6282-1670)
Shazia Ali
Andrea T. Hooper (ORCID: https://orcid.org/0000-0003-1131-1229)
Cynthia X. Pan (ORCID: https://orcid.org/0000-0003-1471-973X)
Biomedical Advanced Research and Development Authority
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article
Assessing the safety and pharmacokinetics of casirivimab and imdevimab (CAS+IMD) in a cohort of pregnant outpatients with COVID-19: results from an adaptive, multicentre, randomised, double-blind, phase 1/2/3 study
John D. Davis, Shazia Ali, Andrea T. Hooper, Cynthia X. Pan et al.
Journal
BMJ Open
Topics
COVID-19 Impact on Reproduction
article
Assessing the safety and pharmacokinetics of casirivimab and imdevimab (CAS+IMD) in a cohort of pregnant outpatients with COVID-19: results from an adaptive, multicentre, randomised, double-blind, phase 1/2/3 study
John D. Davis, Shazia Ali, Andrea T. Hooper, Cynthia X. Pan, Ned Braunstein, Samit Ganguly, Jesse T. Chao, Edward Cox, Rafia Bhore, Thomas Norton, Mazhar Thakur, Jennifer D. Hamilton, Paula Dakin, Danise Subramaniam, Bari Kowal, Gregory P. Geba, Joseph A. Bocchini, Alpana Waldron, Gary Herman, Jing Xiao, Yogesh S. Patel, Dominique Atmodjo-Watkins, K. C. Turner, A. Thomas DiCioccio, Susan C. Irvin
article en
Abstract
No abstract available for this paper.
Publication Tag
BMJ OpenVol. 14(10)
Institutions
Regeneron (United States) (US), Willis-Knighton Cancer Center (US)
Funders
U.S. Department of Health and Human Services, F. Hoffmann-La Roche, Regeneron Pharmaceuticals, Biomedical Advanced Research and Development Authority