Study identifier:D7870C00001
ClinicalTrials.gov identifier:NCT03001297
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase 1 Randomized, Blinded, Placebo-controlled Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Single-Ascending Doses of MEDI5884 in Healthy Volunteers
Healthy Volunteers
Phase 1
Yes
-
All
64
Interventional
18 Years - 55 Years
Allocation: Randomized
Endpoint Classification: Safety/Efficacy
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Sept 2019 by MedImmune, LLC
MedImmune, LLC
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: MEDI5884 Dose 1 Participants will receive single dose of MEDI5884 Dose 1 injection SC on Day 1. | Biological/Vaccine: MEDI5884 Dose 1 Participants will receive single dose MEDI5884 Dose 1 injection SC on Day 1. |
Placebo Comparator: Placebo Placebo will be administered subcutaneously (SC). | Biological/Vaccine: Placebo Participants will receive single dose of placebo matched MEDI5884 injection SC on Day 1 |
Experimental: MEDI5884 Dose 2 Participants will receive single dose of MEDI5884 Dose 2 injection SC on Day 1. | Biological/Vaccine: MEDI5884 Dose 2 Participants will receive single dose MEDI5884 Dose 2 injection SC on Day 1 |
Experimental: MEDI5884 Dose 3 Participants will receive single dose of MEDI5884 Dose 3 injection SC on Day 1. | Biological/Vaccine: MEDI5884 Dose 3 Participants will receive single dose MEDI5884 Dose 3 injection SC on Day 1 |
Experimental: MEDI5884 Dose 4 Participants will receive single dose of MEDI5884 Dose 4 injection SC on Day 1. | Biological/Vaccine: MEDI5884 Dose 4 Participants will receive single dose MEDI5884 Dose 4 injection SC on Day 1 |