Among a cohort of patients who received the drug, most improved, but there was no comparison group.
Remdesivir, an inhibitor of viral RNA polymerase, has activity against SARS-CoV-2 (the cause of COVID-19) in vitro and against other betacoronaviruses in animal models. Now, the results of a manufacturer-funded case series of people with COVID-19 who received remdesivir through a compassionate-use program are published.
A total of 61 hospitalized patients with severe disease in the U.S., Canada, Europe, and Japan received intravenous remdesivir, but only 53 were evaluated; the rest did not have posttreatment data or had a dosing error. Before receiving remdesivir, patients' median symptom duration was 12 days, 57% were receiving mechanical ventilation, and 8% were on extracorporeal membrane oxygenation (ECMO).
Outcomes at a median of 18 days …
Reviewing Author
DisclosuresGrant/Research SupportNIH
Editorial BoardsUpToDate; ID Images (idimages.org); Infectious Diseases Society of America COVID-19 Treatment Guidelines; International Antiviral Society–USA (Guidelines Committee)
Leadership Positions in Professional SocietiesHIV Medicine Association; Infectious Diseases Society of America (Board of Directors)
DisclosuresGrant/Research SupportNIH
Editorial BoardsUpToDate; ID Images (idimages.org); Infectious Diseases Society of America COVID-19 Treatment Guidelines; International Antiviral Society–USA (Guidelines Committee)
Leadership Positions in Professional SocietiesHIV Medicine Association; Infectious Diseases Society of America (Board of Directors)