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[157] In April 2021, the FDA revoked the emergency use authorization (EUA) that allowed and signaled FDA agreement for the investigational monoclonal antibody therapy bamlanivimab, when administered alone, to be used for the treatment of mild-to-moderate COVID-19 in adults and certain pediatric patients
Cycle 8 to 12 weeks on, 4 weeks off
EP: HELSINGIN YLIOPISTO OP - FI 20205738 A OP - FI 2021050529 W
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Endocrinology 149, 40594068
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