A Neutralizing Monoclonal Antibody for Hospitalized Patients with Covid-19: bamlanivimab
Principal Investigator(s): View help for Principal Investigator(s) Jens D Lundgren, Department of Infectious Diseases, Rigshospitalet, Copenhagan, Denmark
Version: View help for Version V1
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Project Citation:
Lundgren, Jens D. A Neutralizing Monoclonal Antibody for Hospitalized Patients with Covid-19: bamlanivimab . Ann Arbor, MI: Inter-university Consortium for Political and Social Research [distributor], 2023-10-24. https://doi.org/10.3886/E194685V1
Project Description
Summary:
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This data comes from a randomized, international, double blind study comparing LY-CoV555 to standard of care for the primary outcome of sustained recovery during a 90-day period in hospitalized patients with COVID-19, carried out in Fall 2020. Participants were randomized 1:1 to receive either Ly-CoV555 or matching placebo. All patients received high-quality supportive care as background therapy, including the use of remdesivir. A total of 314 patients were enrolled, 163 to LY-CoV555 and 151 to placebo. The rate ratio for sustained recovery was 1.06 (95% CI, 0.77 to 1.47).
Funding Sources:
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Operation Warp Speed)
Scope of Project
Subject Terms:
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Monoclonal Antibody;
bamlanivimab;
COVID-19;
Randomized clinical trial;
sustained recovery
Geographic Coverage:
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United States, Denmark
Time Period(s):
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8/1/2020 – 1/31/2021 (Fall 2020)
Collection Date(s):
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8/1/2020 – 1/31/2021
Universe:
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COVID-19 hospitalized patients age 18 and over
Data Type(s):
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clinical data;
program source code
Collection Notes:
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SAS datasets and item documentation
Methodology
Response Rate:
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Response rate was not collected. Only participants that consented had data collected.
Response rate was not collected. Only participants that consented had data collected.
Sampling:
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Hospitalized patients with COVID-19
Hospitalized patients with COVID-19
Data Source:
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Clinical trial database
Collection Mode(s):
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coded on-site observation;
face-to-face interview;
other;
telephone interview
Scales:
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No scales used. Primary endpoint was sustained recovery; discharged to home and remaining home for 14 consecutive days.
Weights:
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No weights used
Unit(s) of Observation:
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individuals
Geographic Unit:
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person level
Related Publications
This study is un-published. See below for other available versions.
Published Versions
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