The Annals of Internal Medicine today published the results from a University of Pittsburgh Medical Center hypothetical randomized study that estimated administering monoclonal antibodies (mAbs) within two days of a COVID-19 diagnosis lowered the risk of hospitalization or death by about 39%.
The risk for hospitalization or death at 28 days was 4.6% in 2571 treated patients and 7.6% in 5135 nontreated control patients (risk ratio [RR], 0.61 [95% CI, 0.50 to 0.74]). In sensitivity analyses, the corresponding RRs for 1- and 3-day treatment grace periods were 0.59 and 0.49, respectively.
In subgroup analyses, those receiving mAbs when the Alpha and Delta variants were presumed to be predominant had estimated RRs of 0.55 and 0.53, respectively, compared with 0.71 for the Omicron variant period.
Relative risk estimates for individual mAb products all suggested a lower risk for hospitalization or death. The RR was 0.45 (CI, 0.28 to 0.71) among immunocompromised patients.
mABS are human-made antibodies designed to prevent a pathogen, such as the coronavirus that causes COVID-19, from entering human cells, replicating, and causing serious illness.
The U.S. Food and Drug Administration granted emergency use authorization to five different COVID-19 mAbs treatments between 2020 and 2022.
As of April 4, 2023, one mAbs (Gohibic) is authorized for use in the U.S.














