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A Phase 1 Study of Cizutamig in IgE Mediated Diseases

C

Candid Therapeutics

Status and phase

Not yet enrolling
Phase 1

Conditions

IgE-Mediated Hypersensitivity
IgE-Mediated Cow Milk Allergy
IgE Mediated Food Allergy

Treatments

Biological: Cizutamig

Study type

Interventional

Funder types

Industry

Identifiers

NCT07408869
CND106-110

Details and patient eligibility

About

The purpose of this study is to evaluate the pharmacodynamics, safety, tolerability, pharmacokinetics, and immunogenicity of cizutamig in IgE Mediated Diseases.

Full description

This is a Phase 1b, open-label study evaluating the pharmacodynamics, safety, tolerability, pharmacokinetics, and immunogenicity of cizutamig in IgE Mediated Diseases.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patient meets at least one of the following:

    1. History of documented (skin prick test, in vitro testing, or food challenge), ongoing, IgE-mediated allergy to food (eg, peanut, hazelnut, walnut, cashew, milk, egg/egg white, soy, wheat, sesame, cod, salmon, tuna, lobster, crab and/or shrimp) with Screening total IgE ≥ 400 IU/mL
    2. Diagnosis of chronic rhinosinusitis with Screening total IgE > ULN
    3. Diagnosis of allergic rhinitis with Screening total IgE > ULN
    4. Diagnosis of asthma and classified as well controlled per 2024 Global Initiative for Asthma guidelines with Screening total IgE > ULN
    5. Diagnosis of chronic spontaneous urticaria with symptoms (eg, wheals or angioedema) for at least 6 weeks any time prior to screening and Screening total IgE > ULN
    6. Diagnosis of atopic dermatitis that has been present for at least 6 months before the screening visit and with Screening total IgE > ULN
  2. Agree to the use of highly effective contraception

Exclusion criteria

  1. Elevated IgE levels for reasons other than the IgE mediated diseases
  2. Planned ingestion of food items to which they are allergic for the duration of the study (for food allergy patients)
  3. Current use of any allergen immunotherapy.
  4. Individuals whose allergen exposures in their home and/or work environments may be expected to change significantly during the trial period
  5. Inadequate clinical laboratory parameters at Screening
  6. Receipt of or inability to discontinue any excluded therapies
  7. Individuals who will decline blood products
  8. Active infection
  9. Serious mental illness, drug or alcohol abuse, dementia, or other condition that impair ability to sign ICF
  10. Individuals who are hypersensitive to intravenous immunoglobulin (IVIg)
  11. History of primary immunodeficiency
  12. History of CNS disease
  13. History of poorly controlled diabetes, chronic kidney disease, chronic pulmonary disease, uncontrolled cardiovascular disease, history of malignancy within 5 years
  14. History of severe allergic or anaphylactic reactions to mAb therapy (or recombination antibody-related fusion proteins) or any constituents of study drug
  15. Major surgery requiring the use of general anesthesia within 12 weeks prior to Screening or planned or expected major surgery during the study period
  16. Blood donation or significant blood loss within 30 days prior to screening
  17. Individuals considered to be part of a vulnerable population (eg, incarceration)
  18. Individuals that in the opinion of the Investigator, are not suitable for participation in the trial
  19. Inability to comply with protocol-mandated requirements
  20. A history of severe allergic or anaphylactic reactions related to the underlying IgE mediated disease

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

20 participants in 2 patient groups

cizutamig (single dose)
Experimental group
Description:
cizutamig will be dosed subcutaneously according to the cohort assignment
Treatment:
Biological: Cizutamig
cizutamig (multiple dose)
Experimental group
Description:
cizutamig will be dosed subcutaneously according to the cohort assignment
Treatment:
Biological: Cizutamig

Trial contacts and locations

1

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Central trial contact

Clinical Operations

Data sourced from clinicaltrials.gov

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