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New drug aims to tame severe allergies by lowering key antibody

NCT ID NCT07408869

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled This study
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

Dec 2026

An estimate. End dates often move.

Lead sponsor

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

18 to 65 years

Sex

Anyone

Healthy volunteers

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

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.

allergic rhinitis asthma atopic eczema chronic idiopathic urticaria chronic rhinosinusitis Egg Hypersensitivity food allergy Hypersensitivity, Immediate IgE responsiveness, atopic Milk Hypersensitivity Nut Hypersensitivity Peanut Hypersensitivity Rhinitis, Allergic Rhinosinusitis urticaria Wheat Hypersensitivity

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Nucleus Network

    Melbourne, Victoria, 3004, Australia

More trials for these conditions

Other studies related to the condition(s) this trial covers.