A Phase 1 Study to Assess the Safety and Immunogenicity of JCXH-221, an MRNA-based Broadly Protective COVID-19 Vaccine

PHASE1CompletedINTERVENTIONAL
Enrollment

73

Participants

Timeline

Start Date

March 7, 2023

Primary Completion Date

December 1, 2023

Study Completion Date

December 1, 2023

Conditions
COVID-19Infectious Disease
Interventions
BIOLOGICAL

JCXH-221

Participants will be randomized to either placebo or JCXH-221 for Phase 1. For Phase 2, participants will either be randomized to JCXH-221 or a FDA approved Active comparator.

OTHER

Placebo

Participants will be randomized in Phase 1 to either JCXH-221 or placebo

Trial Locations (4)

31406

Velocity Clinical Research, Savannah

33009

Velocity Clinical Research, Hallandale

68510

Velocity Clinical Research, Lincoln

78613

Velocity Clinical Research, Cedar Park

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

ICON plc

INDUSTRY

lead

Immorna Biotherapeutics, Inc.

INDUSTRY