A Study of NN2802, an Anti-c-Kit Antibody, in Healthy Participants and in Adults With Chronic Spontaneous Urticaria (CSU)
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.
研究概览
研究类型
注册 (估计的)
阶段
- 阶段2
- 阶段1
联系人和位置
学习联系方式
- 姓名:Clinical Study Lead
- 电话号码:1 617.870.7173
- 邮箱:NN2802@noveltynobility.com
学习地点
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Hangzhou、中国
- 招聘中
- Hangzhou First People's Hospital
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接触:
- Ying WANG, MD
- 电话号码:+86-18367124548
- 邮箱:nancywangying@163.com
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria(Part A):
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Participants must sign an IRB/IEC approved informed consent form before any study specific procedures are performed.
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Healthy adult male and female participants between 18 and 65 years of age, inclusive, at the time of screening.
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Participants must have suitable veins for cannulation or repeated venipuncture.
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If female, meets one the of following criteria:
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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
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Is of non-childbearing potential, defined as surgically sterile, or is in a postmenopausal state.
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If male, meets one the following criteria:
- Abstinence from penile vaginal intercourse as their usual and preferred lifestyle.
- Unable to procreate, defined by surgically sterile
- Agrees to use male condom when having sexual intercourse with a woman of childbearing potential.
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Body mass index (BMI) between 18.0 and 26.0 kg/m2, inclusive.
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Normal or clinically acceptable physical examination, clinical laboratory test values, ECG, and vital signs, as determined by the Investigator.
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Total bilirubin, ALT, AST and creatinine ≤ upper limit of normal (ULN).
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No known history of active tuberculosis.
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Participant has a negative tuberculosis test at screening
Inclusion Criteria(Part B):
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Participants must sign an IRB/IEC approved ICF before any study-specific procedures are performed.
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Adult male and female participants between 18 and 75 years of age, inclusive, at the time of screening.
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Weight ≥40 kg.
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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:
- CSU diagnosis ≥ 6 months, with supporting documentation
- 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.
- UAS7 (range 0-42) of ≥16 and ISS7 (range 0-21) of ≥8 during the 7 days before treatment.
- 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.
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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.
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If female, meets one the of following criteria:
- Is of childbearing potential and agrees to use a highly effective contraceptive method. OR
- Is of non-childbearing potential, defined as surgically sterile, or is in a postmenopausal state.
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If male, meets one the following criteria:
- Abstinence from penile vaginal intercourse as their usual and preferred lifestyle.
- Unable to procreate, defined by surgically sterile
- Agrees to use male condom when having sexual intercourse with a woman of childbearing potential.
Exclusion Criteria(Part A):
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Female who is lactating.
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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.
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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.
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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.
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Positive drugs of abuse (including marijuana) or alcohol screen test.
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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.
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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:
- any non-prescribed (i.e., over-the-counter) systemic or topical medication.
- any herbal remedy, vitamin, or mineral supplement.
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Participants who have received:
- 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.
- any antihistamines within 5 half-lives prior to dosing.
- immunosuppressive drugs within 60 days prior to dosing.
- COVID-19 vaccination within 30 days prior to dosing.
- standard vaccinations within 14 days prior to dosing or other live or live-attenuated vaccine 3 months prior to dosing.
- 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.
- for male participants, medications that are known to affect sperm count or motility within 30 days prior to dosing
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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.
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History of anaphylaxis, clinically significant drug allergies or allergic conditions (excluding non-active seasonal allergies), as determined by the Investigator.
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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).
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Participants who have previously received NN2802.
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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.
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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.
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Recent infection (within 3 months prior to dosing) requiring inpatient hospitalization or IV antibiotics.
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Clinically significant illness, medical/surgical procedure, or trauma within 4 weeks prior to dosing, as determined by the Investigator.
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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.
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Infectious Disease Risk
Participants will be excluded if any of the following apply at screening:
- Positive test for HIV (Human immunodeficiency virus) antibodies.
- Positive or indeterminate HBsAg, or positive IgM HBcAb, or positive Total HBcAb and positive HBV DNA, or positive HCV Ab and positive HCV RNA.
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Received or scheduled to receive a live vaccination within 3 months prior to dosing and until 3 months following study drug dosing.
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Previously enrolled in or withdrawn from this study.
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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.
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Participants who, in the opinion of the Investigator, should not participate in this study.
Exclusion Criteria(Part B):
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Clearly defined cause for chronic urticaria, including any of the following:
- Symptomatic solar-, cholinergic-, heat-, cold-, aquagenic- or contact induced urticaria, artificial urticaria, symptomatic urticaria or vibratory angioedema
- 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
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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.
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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.
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Participants who have received:
- immunosuppressive drugs (e.g., cyclosporine, tacrolimus) within 60 days prior to dosing.
- COVID-19 vaccination within 30 days prior to dosing.
- Standard vaccinations within 14 days prior to dosing or other live or live attenuated vaccine 3 months prior to dosing.
- Previous use of IgE therapy (e.g., Omalizumab) within 5 half-lives of the respective anti-IgE therapy prior to dosing.
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Anticipated requirement for the use of any leukotriene receptor antagonist (Montelukast, Zafirlukast) use between Day 1 and EOS (inclusive).
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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.
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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.
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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).
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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).
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History of hypersensitivity or allergy to NN2802 or its excipients.
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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.
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Known or clinically suspected active helminthic parasitic infection, as determined by the Investigator based on medical history and clinical presentation.
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Active infection or history of infection as follows:
- Any active infection for which oral anti-infectives (antibiotics, antivirals, antifungals) were used ≤ 14 days prior to first dose of study drug).
- A serious infection requiring hospitalization or IV anti-infectives (antibiotics, antivirals, antifungals) ≤ 30 days prior to first dose of study drug.
- 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.
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Clinically significant illness, medical/surgical procedure, or trauma within 4 weeks prior to dosing, as determined by the Investigator.
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Infectious Disease Risk
Participants will be excluded if any of the following apply at screening:
- Positive test for HIV (Human immunodeficiency virus) antibodies.
- Positive or indeterminate HBsAg, or positive IgM HBcAb, or positive Total HBcAb and positive HBV DNA, or positive HCV Ab and positive HCV RNA.
- Tuberculosis (TB) risk
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Laboratory abnormalities at screening:
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Clinically significant electrocardiogram (ECG) findings unless approved by Cardiologist or Study Medical Monitor.
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Received or scheduled to receive a live vaccination within 3 months prior to dosing and until 3 months following study drug dosing.
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Previously enrolled in or withdrawn from this study.
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Active substance abuse (drug or alcohol) within 24 weeks prior to first dose of study drug, as determined by the investigator.
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Inability or unwillingness to be available for follow-up visits or protocol required procedures.
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Participants who, in the Investigator's opinion, should not participate in this study.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Part A-1
NN2802 Dose 1 or placebo administered intravenously once |
Investigational product |
|
实验性的:Part A-2
NN2802 Dose 2 or placebo administered intravenously once |
Investigational product |
|
实验性的:Part B-1
NN2802 Dose 1 administered intravenously Q8W |
Investigational product |
|
实验性的:Part B-2 High
NN2802 Dose administered intravenously Q8W or Q4W |
Investigational product |
|
实验性的:Part B-2 Mid
NN2802 Dose administered intravenously Q8W or Q4W |
Investigational product |
|
实验性的:Part B-2 Low
NN2802 Dose administered intravenously Q8W or Q4W |
Investigational product |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Part A: Incidence of Adverse Events
大体时间: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
大体时间:22 weeks
|
Safety parameters [adverse events (AEs), physical examinations, vital signs, electrocardiograms (ECG findings), and laboratory values. |
22 weeks
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Part A: Pharmacokinetics (PK) of NN2802
大体时间:14 weeks
|
PK parameters by measureing serum concentration of NN2802 |
14 weeks
|
|
Part A: Pharmacodynamics(PD) of NN2802
大体时间:14 weeks
|
Change in biomarkers such as serum tryptase. |
14 weeks
|
|
Part B: Pharmacokinetics (PK)of NN2802
大体时间:22 weeks
|
PK parameters by measureing serum concentration of NN2802 |
22 weeks
|
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Part B: Pharmacodynamics(PD) of NN2802
大体时间:22 weeks
|
Change in biomarkers such as serum tryptase. |
22 weeks
|
|
Part B: Change from baseline of UAS7 over time.
大体时间:22 weeks
|
22 weeks
|
|
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Part B: Change from baseline of ISS7 over time.
大体时间:22 weeks
|
22 weeks
|
|
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Part B: Change from baseline of HSS7 over time.
大体时间:22 weeks
|
22 weeks
|
|
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Part B: Change from baseline of CU-Q2oL over time.
大体时间:22 weeks
|
22 weeks
|
|
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Part B: Change from baseline of UCT over time.
大体时间:22 weeks
|
22 weeks
|
|
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Part B: Proportion of participants achieving UAS7=0 over time.
大体时间:22 weeks
|
22 weeks
|
|
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Part B: Cumulative number of weeks that participants achieve an AAS7 score=0 after baseline and over time.
大体时间:22 weeks
|
22 weeks
|
其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Part A: Immunogenicity of NN2802
大体时间:14 weeks
|
Immunogenicity assessed by ADA analyses |
14 weeks
|
|
Part A: Additional PD biomarkers
大体时间: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
大体时间:22 weeks
|
Immunogenicity assessed by ADA analyses |
22 weeks
|
|
Part B: Additional PD biomarkers
大体时间:22 weeks
|
Change in biomarkers including but not limited to s-SCF and skin biopsy. |
22 weeks
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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