Phase 1, Randomized, Double-Blind, Placebo-controlled Study to Evaluate the Safety and Tolerability of an Enterovirus D68-specific Monoclonal Antibody in Healthy Adults

PHASE1CompletedINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

June 26, 2024

Primary Completion Date

April 11, 2025

Study Completion Date

April 11, 2025

Conditions
Enterovirus Infection
Interventions
BIOLOGICAL

EV68-228-N

EV68-228-N is a recombinant human monoclonal IgG1 antibody which is produced by genetically engineered plasmids in Nicotiana benthamiana. This intervention is directed against enterovirus EV-D68 capsid protein potentially providing treatments for EV-D68 infection and AMF.

OTHER

Placebo for EV68-228-N

The placebo is a sterile buffer solution formulated to match the EV68-228-N Drug Product. The formulation is 20mM Citrate + 10 mM Glycine, 8% Sucrose, and 0.01% Polysorbate 80, with a target pH of 5.5. The placebo will be filled into glass vials at 10 mL per vial. The formulation buffer is a clear colorless liquid.

Trial Locations (2)

21201-1509

University of Maryland, School of Medicine, Center for Vaccine Development and Global Health, Baltimore

37232-0011

Vanderbilt University Medical Center, Nashville

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

KBio Inc

INDUSTRY

lead

National Institute of Allergy and Infectious Diseases (NIAID)

NIH