Covance Clinical Research Inc
Daytona Beach, Florida, 32117, United States
NCT Number: NCT04611789
The purpose of this study is to test the safety and tolerability of LY3832479 when it is given by injection just under the skin to healthy participants. Blood tests will be done to check how much LY3832479 is in the bloodstream and how long the body takes to eliminate it. Participation could last up to 16 weeks and may include up to six visits to the study center, with a one-week overnight stay.
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Notify Me18 year–60 year
All sexes
Interventional
Phase 1
Daytona Beach, Florida, 32117, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Administered subcutaneously
Other names: LY-CoV016, Etesevimab
Administered subcutaneously
Time frame: Day 1, 2, 3, 4, 5, 6, 7, 15, 29, 60 and 85 postdose
Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve from Time 0 to tlast (AUC[0-tlast]) of LY3832479.
Time frame: Day 1, 2, 3, 4, 5, 6, 7, 15, 29, 60 and 85 postdose
PK: Maximum Serum Concentration (Cmax) of LY3832479.
Eli Lilly and Company
Industry
A Randomized, Placebo-Controlled, Participant- and Investigator-Blind, Phase 1 Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of LY3832479 Administered Subcutaneously to Healthy Participants
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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