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Compassionate Use of Remdesivir for Patients with Severe Covid-19.
- Source :
-
The New England journal of medicine [N Engl J Med] 2020 Jun 11; Vol. 382 (24), pp. 2327-2336. Date of Electronic Publication: 2020 Apr 10. - Publication Year :
- 2020
-
Abstract
- Background: Remdesivir, a nucleotide analogue prodrug that inhibits viral RNA polymerases, has shown in vitro activity against SARS-CoV-2.<br />Methods: We provided remdesivir on a compassionate-use basis to patients hospitalized with Covid-19, the illness caused by infection with SARS-CoV-2. Patients were those with confirmed SARS-CoV-2 infection who had an oxygen saturation of 94% or less while they were breathing ambient air or who were receiving oxygen support. Patients received a 10-day course of remdesivir, consisting of 200 mg administered intravenously on day 1, followed by 100 mg daily for the remaining 9 days of treatment. This report is based on data from patients who received remdesivir during the period from January 25, 2020, through March 7, 2020, and have clinical data for at least 1 subsequent day.<br />Results: Of the 61 patients who received at least one dose of remdesivir, data from 8 could not be analyzed (including 7 patients with no post-treatment data and 1 with a dosing error). Of the 53 patients whose data were analyzed, 22 were in the United States, 22 in Europe or Canada, and 9 in Japan. At baseline, 30 patients (57%) were receiving mechanical ventilation and 4 (8%) were receiving extracorporeal membrane oxygenation. During a median follow-up of 18 days, 36 patients (68%) had an improvement in oxygen-support class, including 17 of 30 patients (57%) receiving mechanical ventilation who were extubated. A total of 25 patients (47%) were discharged, and 7 patients (13%) died; mortality was 18% (6 of 34) among patients receiving invasive ventilation and 5% (1 of 19) among those not receiving invasive ventilation.<br />Conclusions: In this cohort of patients hospitalized for severe Covid-19 who were treated with compassionate-use remdesivir, clinical improvement was observed in 36 of 53 patients (68%). Measurement of efficacy will require ongoing randomized, placebo-controlled trials of remdesivir therapy. (Funded by Gilead Sciences.).<br /> (Copyright © 2020 Massachusetts Medical Society.)
- Subjects :
- Adenosine Monophosphate adverse effects
Adenosine Monophosphate therapeutic use
Administration, Intravenous
Adult
Aged
Aged, 80 and over
Alanine adverse effects
Alanine therapeutic use
Antiviral Agents adverse effects
Betacoronavirus
COVID-19
Canada
Coronavirus Infections mortality
Europe
Female
Humans
Japan
Male
Middle Aged
Pandemics
Pneumonia, Viral mortality
Respiration, Artificial
SARS-CoV-2
United States
Young Adult
COVID-19 Drug Treatment
Adenosine Monophosphate analogs & derivatives
Alanine analogs & derivatives
Antiviral Agents therapeutic use
Compassionate Use Trials
Coronavirus Infections drug therapy
Pneumonia, Viral drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1533-4406
- Volume :
- 382
- Issue :
- 24
- Database :
- MEDLINE
- Journal :
- The New England journal of medicine
- Publication Type :
- Academic Journal
- Accession number :
- 32275812
- Full Text :
- https://doi.org/10.1056/NEJMoa2007016