Remternetug (Test)
DrugAdministered SC
Other names: LY3372993
NCT Number: NCT07056309
The main purpose of this study is to evaluate to different formulations of remternetug after single subcutaneous (SC) administration with either an autoinjector (AI) or a prefilled syringe (PFS). The study will look at the amount of remternetug that gets into the bloodstream and how long it takes the body to get rid of the remternetug when given as two different formulations.
Participation in the study will last approximately 155 days.
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Notify Me18 year–45 year
All sexes
Interventional
Phase 1
Fortrea Clinical Research Unit, Daytona Beach, Florida, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Administered SC
Other names: LY3372993
Administered SC
Other names: LY3372993
Time frame: Predose up to Day 85
Time frame: Predose up to Day 85
Time frame: Predose up to Day 85
Time frame: Predose up to Day 85
Eli Lilly and Company
Industry
A Study on Pharmacokinetics of Remternetug Administered Subcutaneously Through an Autoinjector Versus Prefilled Syringe in Healthy Participants
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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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