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RECRUITING
NCT07236411
PHASE1

Absolute Bioavailability Study of Cizutamig in Healthy Adult Participants

Sponsor: Candid Therapeutics

View on ClinicalTrials.gov

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

Interventions

BIOLOGICAL

cizutamig

cizutamig will be dosed SC or IV according to the assigned cohort

OTHER

Placebo

placebo will be dosed IV or SC according to the assigned cohort

Locations (1)

Nucleus Network

Melbourne, Victoria, Australia