New drug aims to tame severe allergies by lowering key antibody
NCT ID NCT07408869
First seen Jun 27, 2026 · Last updated Jul 23, 2026 · Updated 2 times
Summary
This early-stage study tests a new drug called cizutamig in about 20 adults with IgE-mediated allergies, including food allergies. The main goal is to see if the drug can safely lower IgE levels, which are antibodies that trigger allergic reactions. Researchers will also monitor side effects and how the drug moves through the body.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Expected to start
-
Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Nucleus Network
Melbourne, Victoria, 3004, Australia
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Other studies related to the condition(s) this trial covers.
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