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COMPLETED
NCT04194892
PHASE1

A Crossover Study to Evaluate Pegilodecakin (LY3500518) in Healthy Participants

Sponsor: Eli Lilly and Company

View on ClinicalTrials.gov

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

Interventions

BIOLOGICAL

Pegilodecakin

Administered SQ

Locations (1)

PPD Phase 1 Clinic

Austin, Texas, United States