ARTICLE | Product Development
Plasma authorization forces rethink of COVID-19 antibody trials
Developers of mAbs against COVID-19 may be compelled to enroll patients receiving convalescent plasma
August 28, 2020 11:52 PM UTC
Individuals who have received or plan to receive convalescent plasma are excluded from ongoing clinical trials of two COVID-19 antiviral mAb therapies — REGn-COV2 from Regeneron and LY-CoV555 from Lilly and AbCellera — that may soon need to change.
The trials were designed before emergency use authorization (EUA) made convalescent plasma therapy a contender for standard of care for COVID-19. ...
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