Remdesivir for the Treatment of Covid-19 — Final Report
National Institute of Allergy and Infectious Diseases
Abstract
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.
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.
Citation impact
- FWCI
- 173.77
- Percentile
- 100%
- References
- 24
Authors
40- JHJohn H. BeigelCorresponding
National Institute of Allergy and Infectious Diseases
- KMKay M Tomashek
National Institute of Allergy and Infectious Diseases
- LELori E. Dodd
National Institute of Allergy and Infectious Diseases
- AKAneesh K. Mehta
National Institute of Allergy and Infectious Diseases
- BSBarry S. Zingman
National Institute of Allergy and Infectious Diseases
Topics & keywords
- Coronavirus disease 2019 (COVID-19)
- 2019-20 coronavirus outbreak
- Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
- Virology
- Medicine
- Internal medicine
- Outbreak
- Good health and well-being
Funding
- UDU.S. Department of Defense
- UDU.S. Department of Health and Human ServicesAward: HHSN261200800001E
- UDU.S. Department of Veterans Affairs
- HMHenry M. Jackson Foundation
- GSGilead SciencesAwards: 75N91019F00130, 75N910D00024
- DODivision of Intramural Research, National Institute of Allergy and Infectious Diseases
- NUNorthwestern University
- UOUniversity of Pittsburgh
- KCKing's College London
- SNSeoul National University
- SNSeoul National University Hospital
- URUniversität Regensburg
- NINational Institutes of HealthAwards: UM1AI148689, 75N91019F00130, UM1AI148685, HHSN261200800001E, UM1AI148573, UM1AI148450, 75N91020F00010, 75N910D00024, UM1AI148452, UM1AI148575, UM1AI148576, UM1AI148684
- USUniformed Services University of the Health SciencesAward: HHSN261200800001E
- FSFeinberg School of Medicine
- MRMedical Research CouncilAward: MC_UU_12023/22
- NCNational Cancer InstituteAwards: 75N91019F00130/75N91020F00010, 75N910D00024, UM1AI148576, 75N91019F00130, UM1AI148685, UM1AI148684, UM1AI148575, HHSN261201500003I, UM1AI148450, UM1AI148689, UM1AI148452, UM1AI148573, HHSN261200800001E 75N910D00024
- NINational Institute of Allergy and Infectious DiseasesAwards: UM1AI148573, UM1AI148684, UM1AI148450, UM1AI148689, UM1AI148575, 75N91020F00010, 75N910D00024, 75N91019F00130, UM1AI148685, HHSN261200800001E, UM1AI148452, UM1AI148576