73
Participants
Start Date
March 7, 2023
Primary Completion Date
December 1, 2023
Study Completion Date
December 1, 2023
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.
Placebo
Participants will be randomized in Phase 1 to either JCXH-221 or placebo
Velocity Clinical Research, Savannah
Velocity Clinical Research, Hallandale
Velocity Clinical Research, Lincoln
Velocity Clinical Research, Cedar Park
Lead Sponsor
Collaborators (1)
ICON plc
INDUSTRY
Immorna Biotherapeutics, Inc.
INDUSTRY