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Remdesivir for the Treatment of Covid-19 - Final Report

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  • John H Beigel
  • Kay M Tomashek
  • Lori E Dodd
  • Aneesh K Mehta
  • Barry S Zingman
  • Andre C Kalil
  • Elizabeth Hohmann
  • Helen Y Chu
  • Annie Luetkemeyer
  • Susan Kline
  • Diego Lopez de Castilla
  • Robert W Finberg
  • Kerry Dierberg
  • Victor Tapson
  • Lanny Hsieh
  • Thomas F Patterson
  • Roger Paredes
  • Daniel A Sweeney
  • William R Short
  • Giota Touloumi
  • David Chien Lye
  • Norio Ohmagari
  • Myoung-Don Oh
  • Guillermo M Ruiz-Palacios
  • Thomas Benfield
  • Gerd Fätkenheuer
  • Mark G Kortepeter
  • Robert L Atmar
  • C Buddy Creech
  • Jens Lundgren
  • Abdel G Babiker
  • Sarah Pett
  • James D Neaton
  • Timothy H Burgess
  • Tyler Bonnett
  • Michelle Green
  • Mat Makowski
  • Anu Osinusi
  • Seema Nayak
  • H Clifford Lane
  • ACTT-1 Study Group Members
  • Birgitte Lindegaard Madsen (Medlem af forfattergruppering)
  • Tomas Østergaard Jensen (Medlem af forfattergruppering)
Vis graf over relationer

BACKGROUND: Although several therapeutic agents have been evaluated for the treatment of coronavirus disease 2019 (Covid-19), no antiviral agents have yet been shown to be efficacious.

METHODS: We conducted a double-blind, randomized, placebo-controlled trial of intravenous remdesivir in adults who were hospitalized with Covid-19 and had evidence of lower respiratory tract infection. Patients were randomly assigned to receive either remdesivir (200 mg loading dose on day 1, followed by 100 mg daily for up to 9 additional days) or placebo for up to 10 days. The primary outcome was the time to recovery, defined by either discharge from the hospital or hospitalization for infection-control purposes only.

RESULTS: A total of 1062 patients underwent randomization (with 541 assigned to remdesivir and 521 to placebo). Those who received remdesivir had a median recovery time of 10 days (95% confidence interval [CI], 9 to 11), as compared with 15 days (95% CI, 13 to 18) among those who received placebo (rate ratio for recovery, 1.29; 95% CI, 1.12 to 1.49; P<0.001, by a log-rank test). In an analysis that used a proportional-odds model with an eight-category ordinal scale, the patients who received remdesivir were found to be more likely than those who received placebo to have clinical improvement at day 15 (odds ratio, 1.5; 95% CI, 1.2 to 1.9, after adjustment for actual disease severity). The Kaplan-Meier estimates of mortality were 6.7% with remdesivir and 11.9% with placebo by day 15 and 11.4% with remdesivir and 15.2% with placebo by day 29 (hazard ratio, 0.73; 95% CI, 0.52 to 1.03). Serious adverse events were reported in 131 of the 532 patients who received remdesivir (24.6%) and in 163 of the 516 patients who received placebo (31.6%).

CONCLUSIONS: Our data show that remdesivir was superior to placebo in shortening the time to recovery in adults who were hospitalized with Covid-19 and had evidence of lower respiratory tract infection. (Funded by the National Institute of Allergy and Infectious Diseases and others; ACTT-1 ClinicalTrials.gov number, NCT04280705.).

OriginalsprogEngelsk
TidsskriftThe New England journal of medicine
Vol/bind383
Udgave nummer19
Sider (fra-til)1813-1826
Antal sider14
ISSN0028-4793
DOI
StatusUdgivet - 5 nov. 2020

Bibliografisk note

Copyright © 2020 Massachusetts Medical Society.

ID: 59909544