A Study of LY3819253 (LY-CoV555) in Participants Hospitalized for COVID-19
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- STATUS
- Recruiting
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- participants needed
- 40
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- sponsor
- Eli Lilly and Company
Summary
The purpose of this study is to test the safety and tolerability of LY3819253 when it is given by injection into a vein to participants hospitalized with COVID-19. Blood tests will be done to check how much LY3819253 is in the bloodstream and how long the body takes to eliminate it. Participation could last about 8 weeks and may include up to 15 visits in the hospital or the home.
Details
Condition | Covid 19 |
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Age | 18years - 75years |
Treatment | Placebo, LY3819253 |
Clinical Study Identifier | NCT04411628 |
Sponsor | Eli Lilly and Company |
Last Modified on | 19 February 2024 |
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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