A Study to Evaluate the Pharmacokinetics in Participants After Dosing With Pegilodecakin (LY3500518)
NCT03267732 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 24
Last updated 2019-04-05
Summary
To evaluate the pharmacokinetics of single and multiple doses of pegilodecakin in healthy participants.
Conditions
- Healthy Adult Subjects
Interventions
- BIOLOGICAL
-
Pegilodecakin
Pegilodecakin Alone
Sponsors & Collaborators
-
ARMO BioSciences
collaborator INDUSTRY - lead INDUSTRY
Principal Investigators
-
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST) · Eli Lilly and Company
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2017-09-05
- Primary Completion
- 2017-10-30
- Completion
- 2017-10-30
- FDA Drug
- Yes
Countries
- United States
Study Locations
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