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A Study of NN2802, an Anti-c-Kit Antibody, in Healthy Participants and in Adults With Chronic Spontaneous Urticaria (CSU)

4 de noviembre de 2026 actualizado por: Novelty Nobility, Inc.

A Phase 1/2a, Randomized, Double-Blind, Placebo-Controlled (With an Open-Label Part B-1 Cohort), Single Dose and Multiple Dose Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of NN2802, in Healthy Participants and in Participants With Chronic Spontaneous Urticaria (CSU) Who Remain Symptomatic Despite Treatment With Antihistamines

NN2802 is a new product that is being developed for treating participants with CSU who remain symptomatic despite treatment with antihistamines. NN2802 is not yet an approved product and it can only be used in an experimental study like this one.

The purpose of this study is to learn more about a new experimental drug called NN2802. NN2802 is an investigational fully human monoclonal antibody that inhibits c-Kit. c-Kit is involved in the survival, development, and activity of mast cells, which are important cells involved in allergic and inflammatory reactions. By inhibiting c-Kit, NN2802 may reduce mast cell numbers and activity and may help improve symptoms of CSU, such as hives, itching, and angioedema.

The study will assess the safety, tolerability, pharmacokinetics (PK, amount of drug in your blood), pharmacodynamics (PD, how the drug affects your body), immunogenicity (whether your body develops antibodies against the study drug), and preliminary efficacy (whether the drug may improve CSU symptoms) of NN2802. It also aims to identify suitable doses and dosing schedules of NN2802 for use in future clinical trials.

This study will be conducted at multiple study sites, involving around 44 to 46 participants in total, including healthy participants and participants with CSU who remain symptomatic despite treatment with antihistamines. The number of participants depends on how well the study participants tolerate the treatment and the number of dose groups studied.

Descripción general del estudio

Estado

Reclutamiento

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Estimado)

46

Fase

  • Fase 2
  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

      • Hangzhou, Porcelana
        • Reclutamiento
        • Hangzhou First People's Hospital
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 75 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria(Part A):

  1. Participants must sign an IRB/IEC approved informed consent form before any study specific procedures are performed.

  2. Healthy adult male and female participants between 18 and 65 years of age, inclusive, at the time of screening.

  3. Participants must have suitable veins for cannulation or repeated venipuncture.

  4. If female, meets one the of following criteria:

    1. Is of childbearing potential and agrees to use a highly effective contraceptive method from at least 28 days prior to the Screening visit through to at least 105 days after study drug administration.

      OR

    2. Is of non-childbearing potential, defined as surgically sterile, or is in a postmenopausal state.

  5. If male, meets one the following criteria:

    1. Abstinence from penile vaginal intercourse as their usual and preferred lifestyle.
    2. Unable to procreate, defined by surgically sterile
    3. Agrees to use male condom when having sexual intercourse with a woman of childbearing potential.
  6. Body mass index (BMI) between 18.0 and 26.0 kg/m2, inclusive.

  7. Normal or clinically acceptable physical examination, clinical laboratory test values, ECG, and vital signs, as determined by the Investigator.

  8. Total bilirubin, ALT, AST and creatinine ≤ upper limit of normal (ULN).

  9. No known history of active tuberculosis.

  10. Participant has a negative tuberculosis test at screening

Inclusion Criteria(Part B):

  1. Participants must sign an IRB/IEC approved ICF before any study-specific procedures are performed.

  2. Adult male and female participants between 18 and 75 years of age, inclusive, at the time of screening.

  3. Weight ≥40 kg.

  4. Diagnosis of CSU refractory to H1-antihistamines used alone or in combination with a leukotriene receptor antagonist, at the time of randomization, as defined by all the following:

    1. CSU diagnosis ≥ 6 months, with supporting documentation
    2. Presence of itch and hives for ≥ 6 consecutive weeks at any time prior to enrollment, including inadequate disease control despite treatment with H1-antihistamines, either alone or in combination with leukotriene receptor antagonists, for at least 2 consecutive weeks during this period.
    3. UAS7 (range 0-42) of ≥16 and ISS7 (range 0-21) of ≥8 during the 7 days before treatment.
    4. In-clinic UAS ≥4 on one of the screening visit days, despite use of H1 antihistamines alone or in combination with H2-antihistamines and or leukotriene receptor antagonist) for CSU.
  5. Prior anti-immunoglobulin E (IgE) therapy is allowed (e.g., omalizumab), with the last dose administered at least 5 half-lives of the respective drug prior to randomization.

  6. If female, meets one the of following criteria:

    1. Is of childbearing potential and agrees to use a highly effective contraceptive method. OR
    2. Is of non-childbearing potential, defined as surgically sterile, or is in a postmenopausal state.
  7. If male, meets one the following criteria:

    1. Abstinence from penile vaginal intercourse as their usual and preferred lifestyle.
    2. Unable to procreate, defined by surgically sterile
    3. Agrees to use male condom when having sexual intercourse with a woman of childbearing potential.

Exclusion Criteria(Part A):

  1. Female who is lactating.

  2. Female who is pregnant according to the pregnancy test at screening or prior to study drug administration or plans to become pregnant during the study or within 105 days following study drug dosing.

  3. Donated blood in the 3 months prior to screening, plasma in the 7 days prior to screening, or platelets in the 6 weeks prior to screening.

  4. Consume more than 14 units of alcohol per week (if male) or consume more than 11 units of alcohol per week (if female), or history of alcohol or drug/chemical abuse within 12 months prior to study drug dosing, as determined by the Investigator.

  5. Positive drugs of abuse (including marijuana) or alcohol screen test.

  6. Participants who smoke more than 9 cigarettes, or equivalent in tobacco per day, or inability to abide by the smoking policy of the clinical research unit.

  7. Participants who have used the following within 7 days of dosing, unless in the opinion of the Investigator the medication will not interfere with the study procedures or compromise safety:

    1. any non-prescribed (i.e., over-the-counter) systemic or topical medication.
    2. any herbal remedy, vitamin, or mineral supplement.
  8. Participants who have received:

    1. any prescribed systemic or topical medication within 14 days or 5 half-lives (whichever is longer) prior to dosing, unless in the opinion of the Investigator the medication will not interfere with the study procedures or compromise safety.
    2. any antihistamines within 5 half-lives prior to dosing.
    3. immunosuppressive drugs within 60 days prior to dosing.
    4. COVID-19 vaccination within 30 days prior to dosing.
    5. standard vaccinations within 14 days prior to dosing or other live or live-attenuated vaccine 3 months prior to dosing.
    6. slow-release medicinal formulations considered to still be active within 14 days or 5 half-lives (whichever is longer) prior to dosing, unless in the opinion of the Investigator the medication will not interfere with the study procedures or compromise safety.
    7. for male participants, medications that are known to affect sperm count or motility within 30 days prior to dosing
  9. Received any medications, including St. John's Wort, known to chronically alter drug absorption or elimination processes, within 30 days prior to dosing, unless in the opinion of the Investigator the medication will not interfere with the study procedures or compromise safety.

  10. History of anaphylaxis, clinically significant drug allergies or allergic conditions (excluding non-active seasonal allergies), as determined by the Investigator.

  11. Is currently participating in another clinical study or has received an investigational medicinal product (IMP) within the following time period prior to dosing: 30 days, 5 half-lives, or twice the duration of the biological effect of the IMP (whichever is longer).

  12. Participants who have previously received NN2802.

  13. History of malignancy within 5 years prior to dosing, except treated and considered cured cutaneous squamous or basal cell carcinoma, in situ cervical cancer, or in situ breast ductal carcinoma.

  14. History or evidence of any bacterial, viral, parasitic, or system fungal infections within 30 days prior to dosing. Exception: a simple, short duration common cold resolved more than 14 days prior to dosing.

  15. Recent infection (within 3 months prior to dosing) requiring inpatient hospitalization or IV antibiotics.

  16. Clinically significant illness, medical/surgical procedure, or trauma within 4 weeks prior to dosing, as determined by the Investigator.

  17. History or evidence of any clinically significant disorder (including psychiatric), condition, or disease that, in the opinion of the Investigator, may pose a risk to participant safety or interfere with the study evaluation, procedures, or completion.

  18. Infectious Disease Risk

    Participants will be excluded if any of the following apply at screening:

    1. Positive test for HIV (Human immunodeficiency virus) antibodies.
    2. Positive or indeterminate HBsAg, or positive IgM HBcAb, or positive Total HBcAb and positive HBV DNA, or positive HCV Ab and positive HCV RNA.
  19. Received or scheduled to receive a live vaccination within 3 months prior to dosing and until 3 months following study drug dosing.

  20. Previously enrolled in or withdrawn from this study.

  21. Inability or unwillingness to reside at the clinical research unit during the confinement period, or inability to be available for follow-up visits or protocol required procedures.

  22. Participants who, in the opinion of the Investigator, should not participate in this study.

Exclusion Criteria(Part B):

  1. Clearly defined cause for chronic urticaria, including any of the following:

    1. Symptomatic solar-, cholinergic-, heat-, cold-, aquagenic- or contact induced urticaria, artificial urticaria, symptomatic urticaria or vibratory angioedema
    2. Diseases with symptoms of urticaria and/or angioedema, such as: urticarial vasculitis, urticaria pigmentosa, erythema multiforme, mastocytosis, hereditary or acquired angioedema, hematological or any other malignancies
  2. History or evidence of any clinically significant disorder (including psychiatric), condition, or disease other than CSU, that, in the opinion of the investigator, may pose a risk to participant safety or interfere with the study evaluation, procedures, or completion.

  3. Females who are lactating, or who are pregnant according to the pregnancy test at screening or prior to study drug administration, or plan to become pregnant during the study.

  4. Participants who have received:

    1. immunosuppressive drugs (e.g., cyclosporine, tacrolimus) within 60 days prior to dosing.
    2. COVID-19 vaccination within 30 days prior to dosing.
    3. Standard vaccinations within 14 days prior to dosing or other live or live attenuated vaccine 3 months prior to dosing.
    4. Previous use of IgE therapy (e.g., Omalizumab) within 5 half-lives of the respective anti-IgE therapy prior to dosing.
  5. Anticipated requirement for the use of any leukotriene receptor antagonist (Montelukast, Zafirlukast) use between Day 1 and EOS (inclusive).

  6. Uncontrolled, clinically significant system disease such as diabetes mellitus, cardiovascular disease including moderate-to-severe heart failure (New York Heart Association class III/IV), moderate-to-severe liver disease, or hypertension, as determined by the Investigator.

  7. History of anaphylaxis, clinically significant drug or food allergies or any other clinically significant allergic conditions (e.g., excluding mild seasonal allergies), as determined by the Investigator.

  8. Is currently participating in another clinical study or has received an investigational medicinal product (IMP) within the following time period prior to dosing: 30 days, five half-lives, or twice the duration of the biological effect of the IMP (whichever is longer).

  9. Participants who have previously received NN2802 or any other c-kit targeting agent within the following time period prior to dosing: 30 days, five half-lives, or twice the duration of the biological effect of the IMP (whichever is longer).

  10. History of hypersensitivity or allergy to NN2802 or its excipients.

  11. History of malignancy within 5 years prior to dosing, except treated and considered cured cutaneous squamous or basal cell carcinoma, in situ cervical cancer, or in situ breast ductal carcinoma.

  12. Known or clinically suspected active helminthic parasitic infection, as determined by the Investigator based on medical history and clinical presentation.

  13. Active infection or history of infection as follows:

    1. Any active infection for which oral anti-infectives (antibiotics, antivirals, antifungals) were used ≤ 14 days prior to first dose of study drug).
    2. A serious infection requiring hospitalization or IV anti-infectives (antibiotics, antivirals, antifungals) ≤ 30 days prior to first dose of study drug.
    3. Recurrent or chronic infections or other active infections that in the opinion of the investigator might cause this study to be detrimental to the participant.
  14. Clinically significant illness, medical/surgical procedure, or trauma within 4 weeks prior to dosing, as determined by the Investigator.

  15. Infectious Disease Risk

    Participants will be excluded if any of the following apply at screening:

    1. Positive test for HIV (Human immunodeficiency virus) antibodies.
    2. Positive or indeterminate HBsAg, or positive IgM HBcAb, or positive Total HBcAb and positive HBV DNA, or positive HCV Ab and positive HCV RNA.
    3. Tuberculosis (TB) risk
  16. Laboratory abnormalities at screening:

  17. Clinically significant electrocardiogram (ECG) findings unless approved by Cardiologist or Study Medical Monitor.

  18. Received or scheduled to receive a live vaccination within 3 months prior to dosing and until 3 months following study drug dosing.

  19. Previously enrolled in or withdrawn from this study.

  20. Active substance abuse (drug or alcohol) within 24 weeks prior to first dose of study drug, as determined by the investigator.

  21. Inability or unwillingness to be available for follow-up visits or protocol required procedures.

  22. Participants who, in the Investigator's opinion, should not participate in this study.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Cuadruplicar

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Part A-1

NN2802 Dose 1 or placebo administered intravenously once

Investigational product

Experimental: Part A-2

NN2802 Dose 2 or placebo administered intravenously once

Investigational product

Experimental: Part B-1

NN2802 Dose 1 administered intravenously Q8W

Investigational product

Experimental: Part B-2 High

NN2802 Dose administered intravenously Q8W or Q4W

Investigational product

Experimental: Part B-2 Mid

NN2802 Dose administered intravenously Q8W or Q4W

Investigational product

Experimental: Part B-2 Low

NN2802 Dose administered intravenously Q8W or Q4W

Investigational product

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Part A: Incidence of Adverse Events
Periodo de tiempo: 14 weeks

Safety parameters [adverse events (AEs), physical examinations, vital signs, electrocardiograms (ECG findings), and laboratory values.

14 weeks
Part B: Incidence of Adverse Events
Periodo de tiempo: 22 weeks

Safety parameters [adverse events (AEs), physical examinations, vital signs, electrocardiograms (ECG findings), and laboratory values.

22 weeks

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Part A: Pharmacokinetics (PK) of NN2802
Periodo de tiempo: 14 weeks

PK parameters by measureing serum concentration of NN2802

14 weeks
Part A: Pharmacodynamics(PD) of NN2802
Periodo de tiempo: 14 weeks

Change in biomarkers such as serum tryptase.

14 weeks
Part B: Pharmacokinetics (PK)of NN2802
Periodo de tiempo: 22 weeks

PK parameters by measureing serum concentration of NN2802

22 weeks
Part B: Pharmacodynamics(PD) of NN2802
Periodo de tiempo: 22 weeks

Change in biomarkers such as serum tryptase.

22 weeks
Part B: Change from baseline of UAS7 over time.
Periodo de tiempo: 22 weeks
22 weeks
Part B: Change from baseline of ISS7 over time.
Periodo de tiempo: 22 weeks
22 weeks
Part B: Change from baseline of HSS7 over time.
Periodo de tiempo: 22 weeks
22 weeks
Part B: Change from baseline of CU-Q2oL over time.
Periodo de tiempo: 22 weeks
22 weeks
Part B: Change from baseline of UCT over time.
Periodo de tiempo: 22 weeks
22 weeks
Part B: Proportion of participants achieving UAS7=0 over time.
Periodo de tiempo: 22 weeks
22 weeks
Part B: Cumulative number of weeks that participants achieve an AAS7 score=0 after baseline and over time.
Periodo de tiempo: 22 weeks
22 weeks

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Part A: Immunogenicity of NN2802
Periodo de tiempo: 14 weeks

Immunogenicity assessed by ADA analyses

14 weeks
Part A: Additional PD biomarkers
Periodo de tiempo: 14 weeks

Change in biomarkers including but not limited to serum-stem cell factor (s-SCF) and skin biopsy

14 weeks
Part B: Immunogenicity of NN2802
Periodo de tiempo: 22 weeks

Immunogenicity assessed by ADA analyses

22 weeks
Part B: Additional PD biomarkers
Periodo de tiempo: 22 weeks

Change in biomarkers including but not limited to s-SCF and skin biopsy.

22 weeks

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

15 de octubre de 2026

Finalización primaria (Estimado)

31 de marzo de 2027

Finalización del estudio (Estimado)

31 de marzo de 2028

Fechas de registro del estudio

Enviado por primera vez

26 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

4 de noviembre de 2026

Publicado por primera vez (Actual)

12 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

12 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

4 de noviembre de 2026

Última verificación

1 de noviembre de 2026

Más información

Términos relacionados con este estudio

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

Sí

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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