Our institution is actively considering the use of the monoclonal antibodies that have received emergency use authorization from the FDA (casirivimab+iimdevimab and/or bamlanivimab). While we have chosen not to plan use for the general population, we'd like to consider use for high-risk populations. Do any other institutions have such policies in place?
Thanks,
Brandon Hayes-Lattin
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Brandon Hayes-Lattin MD
Oregon Health & Science Univ
Portland OR
(503) 494-8534
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