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Absolute Bioavailability Study of Cizutamig in Healthy Adult Participants
Sponsor: Candid Therapeutics
Summary
The purpose of this study is to determine the absolute bioavailability of SC administered cizutamig in healthy adult participants.
Official title: A Randomized, Double-blind, Phase 1 Study to Evaluate the Absolute Bioavailability of Cizutamig Following Single Intravenous or Subcutaneous Administration in Healthy Adult Participants
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
20
Start Date
2025-12-04
Completion Date
2026-03
Last Updated
2025-12-26
Healthy Volunteers
Yes
Conditions
Interventions
cizutamig
cizutamig will be dosed SC or IV according to the assigned cohort
Placebo
placebo will be dosed IV or SC according to the assigned cohort
Locations (1)
Nucleus Network
Melbourne, Victoria, Australia