RecruitingPhase 1NCT07236411
Absolute Bioavailability Study of Cizutamig in Healthy Adult Participants
A Randomized, Double-blind, Phase 1 Study to Evaluate the Absolute Bioavailability of Cizutamig Following Single Intravenous or Subcutaneous Administration in Healthy Adult Participants
Sponsor
Candid Therapeutics
Enrollment
20 participants
Start Date
Dec 4, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
The purpose of this study is to determine the absolute bioavailability of SC administered cizutamig in healthy adult participants.
Eligibility
Min Age: 18 YearsMax Age: 65 Years
Inclusion Criteria6
- 18-65 years of age
- Body mass index 18-30 kg/m2 and weight 55-100 kg
- Individuals in good health
- Meets vaccination requirements as defined by the protocol
- Agree to abstain from consumption of alcohol within 48-hrs of study visits
- Agree to the use of highly effective contraception as defined by the protocol
Exclusion Criteria13
- Active Infection
- Inadequate clinical laboratory parameters at Screening
- Receipt of or inability to discontinue any excluded therapies
- Individuals who will decline blood products
- Individuals with immediate household contacts with young children (eg, ≤ 6 years old) or immunocompromised persons
- History of drug or alcohol abuse within last 12 months
- Individuals who are hypersensitive to intravenous immunoglobulin (IVIg)
- History of severe allergic or anaphylactic reactions to mAb therapy (or recombination antibody-related fusion proteins) or any constituents of study drug
- Major surgery requiring the use of general anesthesia within 12 weeks prior to Screening or planned or expected major surgery during the study period (from Screening to the individual's last visit)
- Blood donation or significant blood loss within 30 days prior to screening
- Individuals considered to be part of a vulnerable population (eg, incarceration)
- Individuals that in the opinion of the Investigator, are not suitable for participation in the trial
- Inability to comply with protocol-mandated requirements
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Interventions
BIOLOGICALcizutamig
cizutamig will be dosed SC or IV according to the assigned cohort
OTHERPlacebo
placebo will be dosed IV or SC according to the assigned cohort
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07236411