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A Crossover Study to Evaluate Pegilodecakin (LY3500518) in Healthy Participants
Sponsor: Eli Lilly and Company
Summary
The purpose of this study is to assess how fast pegilodecakin gets into the blood stream and how long it takes the body to remove it, when given as a solution formulation via a prefilled syringe (PFS) versus from a vial drawn into a conventional syringe. Information about side effects will be collected. The study is open to healthy participants. Total participant duration in trial is approximately 42 days.
Official title: An Open Label, Randomized, Single Dose, 2-Way Crossover Study to Evaluate the Pharmacokinetics of Pre-filled Syringe Versus Vial Formulations of AM0010 in Healthy Adult Subjects
Key Details
Gender
All
Age Range
18 Years - 55 Years
Study Type
INTERVENTIONAL
Enrollment
12
Start Date
2018-01-19
Completion Date
2018-03-14
Last Updated
2026-07-13
Healthy Volunteers
Yes
Conditions
Interventions
Pegilodecakin
Administered SQ
Locations (1)
PPD Phase 1 Clinic
Austin, Texas, United States