- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT06311682
Исследование по оценке эффективности и безопасности тралокинумаба в комбинации с местными кортикостероидами у детей и младенцев с атопическим дерматитом средней и тяжелой степени (TRAPEDS 2)
Многоцентровое исследование фазы 3 по оценке эффективности и безопасности тралокинумаба в комбинации с местными кортикостероидами у детей (в возрасте от 2 до 2 лет).
The purpose of this trial is to test whether treatment with tralokinumab (administered subcutaneous injections [SC]) in combination with topical corticosteroids (TCS) is safe and effective to treat moderate-to-severe atopic dermatitis (AD) in children and infants. This will be judged by a range of assessments that rate the severity and extent of atopic dermatitis and its symptoms, as well as general health status and quality of life. The trial will last for up to 4 years. There will be visits every 2 weeks for the first year and every 6 weeks thereafter. Some of the visits will be conducted by phone.
The study involves two different age groups: children aged 2 to under 12 years and infants aged 6 months to under 2 years. This trial compares tralokinumab +TCS to placebo + TCS for children with moderate-to-severe AD and evaluates tralokinumab + TCS for infants with moderate-to-severe AD. Infants will not receive placebo. All subjects will go through a screening process, which is the first part of the trial and will last up to 4 weeks. During this period, it will be checked if the child or infant meets the criteria to participate in the trial.
The children will be randomly assigned to receive tralokinumab + TCS or placebo + TCS for the initial 16 weeks, with the treatment being double-blinded. During the first 16 weeks, children will have a 2 out of 3 chance of getting tralokinumab and a 1 out of 3 chance of getting placebo. Thereafter, all subjects will receive tralokinumab + TCS. The infants will receive tralokinumab + TCS as open-label treatment for the entire treatment period, meaning that the participants will know they are receiving tralokinumab. After stopping treatment, all participants will enter a 4-week safety follow-up period.
Обзор исследования
Статус
Условия
Вмешательство/лечение
Тип исследования
Регистрация (Оцененный)
Фаза
- Фаза 3
Контакты и местонахождение
Контакты исследования
- Имя: Clinical Disclosure
- Номер телефона: +45 4494 5888
- Электронная почта: disclosure@leo-pharma.com
Места учебы
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Brussels, Бельгия, 1020
- Отозван
- Leo Pharma Investigational site
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Ghent, Бельгия, 9000
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Leuven, Бельгия, 3000
- Отозван
- Leo Pharma Investigational site
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Liège, Бельгия, 4000
- Отозван
- Leo Pharma Investigational site
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Buxtehude, Германия, 21614
- Отозван
- Leo Pharma Investigational site
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Dresden, Германия, 01307
- Отозван
- Leo Pharma Investigational site
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Mainz, Германия, 55131
- Отозван
- Leo Pharma Investigational site
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Osnabrück, Германия, 49074
- Отозван
- Leo Pharma Investigational site
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Tübingen, Германия, 72076
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Wuppertal, Германия, 42283
- Отозван
- Leo Pharma Investigational site
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Cork, Ирландия, T12 DFK4
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Crumlin, Ирландия, D12N512
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Alicante, Испания, 03010
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Madrid, Испания, 28046
- Отозван
- Leo Pharma Investigational site
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Valencia, Испания, 46014
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Ancona, Италия, 60126
- Отозван
- Leo Pharma Investigational site
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Brescia, Италия, 25123
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Padova, Италия, 35128
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Roma, Италия, 00168
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Rome, Италия, 00165
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Burlington, Канада, L7L 6W6
- Рекрутинг
- Leo Pharma Investigational site
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Calgary, Канада, Calgary
- Отозван
- Leo Pharma Investigational site
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Calgary, Канада, T2J 7E1
- Рекрутинг
- Leo Pharma Investigational site
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Edmonton, Канада, T5J 3S9
- Рекрутинг
- Leo Pharma Investigational site
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Edmonton, Канада, T6G 1C3
- Рекрутинг
- Leo Pharma Investigational site
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Hamilton, Канада, L8S 1G5
- Рекрутинг
- Leo Pharma Investigational site
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Niagara Falls, Канада, L2H 1H5
- Рекрутинг
- Leo Pharma Investigational site
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Saskatoon, Канада, S7K 2C1
- Рекрутинг
- Leo Pharma Investigational site
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Windsor, Канада, N8X2G1
- Рекрутинг
- Leo Pharma Investigational site
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Winnipeg, Канада, R3M 3Z4
- Рекрутинг
- Leo Pharma Investigational site
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Utrecht, Нидерланды, 3584 CW
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Gdansk, Польша, 80-546
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Krakow, Польша, 30-002
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Lodz, Польша, 90-436
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Ostrowiec Świętokrzyski, Польша, 27-400
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Rzeszów, Польша, 35-055
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Tarnów, Польша, 33-100
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Warsaw, Польша, 02-953
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Warsaw, Польша, 02-962
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Brasov, Румыния, 500091
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Iași, Румыния, 700259
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Lincoln, Соединенное Королевство, LN2 5QY
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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London, Соединенное Королевство, WC1N 3JH
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Sheffield, Соединенное Королевство, S10 2TH
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Southampton, Соединенное Королевство, SO16 6YD
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Alabama
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Birmingham, Alabama, Соединенные Штаты, 35209
- Рекрутинг
- Leo Pharma Investigational site
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Arkansas
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North Little Rock, Arkansas, Соединенные Штаты, 72117
- Рекрутинг
- Leo Pharma Investigational site
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California
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Palo Alto, California, Соединенные Штаты, 94304
- Рекрутинг
- Leo Pharma Investigational site
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Sacramento, California, Соединенные Штаты, 95816
- Рекрутинг
- Leo Pharma Investigational site
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San Diego, California, Соединенные Штаты, 92108
- Отозван
- Leo Pharma Investigational site
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San Diego, California, Соединенные Штаты, 92123
- Рекрутинг
- Leo Pharma Investigational site
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Florida
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Jacksonville, Florida, Соединенные Штаты, 32256
- Рекрутинг
- Leo Pharma Investigational site
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Miami, Florida, Соединенные Штаты, 33156
- Рекрутинг
- Leo Pharma Investigational site
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Tampa, Florida, Соединенные Штаты, 33613
- Рекрутинг
- Leo Pharma Investigational site
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Georgia
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Macon, Georgia, Соединенные Штаты, 31217
- Рекрутинг
- Leo Pharma Investigational site
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Michigan
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Waterford, Michigan, Соединенные Штаты, 48328
- Рекрутинг
- Leo Pharma Investigational site
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Oklahoma
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Tulsa, Oklahoma, Соединенные Штаты, 74136
- Рекрутинг
- Leo Pharma Investigational site
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Oregon
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Portland, Oregon, Соединенные Штаты, 97239
- Рекрутинг
- Leo Pharma Investigational site
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South Carolina
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Charleston, South Carolina, Соединенные Штаты, 27420
- Рекрутинг
- Leo Pharma Investigational site
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Virginia
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Norfolk, Virginia, Соединенные Штаты, 23502
- Рекрутинг
- Leo Pharma Investigational site
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Rijeka, Хорватия, 51000
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Zagreb, Хорватия, 10000
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Zagreb, Хорватия, 10000
- Отозван
- Leo Pharma Investigational site
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Ansan-si, Южная Корея, 15355
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Gwangju, Южная Корея, 61453
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Seoul, Южная Корея, 02447
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Seoul, Южная Корея, 03080
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Seoul, Южная Корея, 03722
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Seoul, Южная Корея, 05030
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Seoul, Южная Корея, 06273
- Отозван
- Leo Pharma Investigational site
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Seoul, Южная Корея, 06591
- Отозван
- Leo Pharma Investigational site
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Seoul, Южная Корея, 139-711
- Активный, не рекрутирующий
- Leo Pharma Investigational site
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Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
Принимает здоровых добровольцев
Полы, имеющие право на обучение
Описание
Inclusion Criteria:
- Age 6 months to <12 years at screening.
- Body weight ≥9 kg at screening.
- Diagnosis of AD as defined by the Hanifin and Rajka (1980) criteria for AD.
- History of AD for: ≥12 months for subjects aged ≥6 years at screening and ≥3 months for subjects aged 6 months to <6 years at screening.
- Documented inadequate response to mid-strength TCS within 6 months before the screening visit.
- AD involvement of ≥10% body surface area at screening and baseline according to component A of SCORAD.
- An EASI score of ≥16 at screening and baseline.
- An IGA score of ≥3 at screening and baseline.
- A Child Worst Itch NRS average score of ≥4 (subjects aged ≥6 years at screening) or a Scratch ObsRO average score of ≥4 (subjects aged <6 years at screening) during the week prior to baseline.
Exclusion Criteria:
- Treatment with the topical corticosteroids (TCS), topical calcineurin inhibitors (TCI), topical phosphodiesterase-4 inhibitors (PDE-4), and topical Janus kinase inhibitors (JAK) within 1 week prior to baseline.
- Treatment with bleach baths within 1 week prior to baseline.
- Treatment with the immunomodulatory medications systemic immunosuppressive/immunomodulating drugs (e.g. methotrexate, cyclosporine, azathioprine, mycophenolate mofetil, Janus kinase inhibitors) and systemic corticosteroids (excludes inhaled, ophthalmic, or intranasal delivery) within 4 weeks prior to baseline.
- Use of tanning beds or phototherapy within 4 weeks prior to baseline.
- Treatment with a live (attenuated) or non-live vaccine within 30 days prior to the baseline visit.
- Active dermatologic conditions that may confound the diagnosis of AD or would interfere with assessment of treatment such as seborrheic dermatitis, active skin infection, scabies, cutaneous T cell lymphoma, or psoriasis.
- Clinically significant active chronic or acute infection requiring treatment with systemic antibiotics, antivirals, antifungals or antiprotozoal within 2 weeks before the baseline visit.
- History of past or current hepatitis B or C including a positive hepatitis B or C test at screening.
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Тройной
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Экспериментальный: Tralokinumab + TCS for subjects aged 2 to <12 years
Dose and dosing frequency for each subject will depend on the subject's body weight. |
The trial medication will be given under the skin (SC). Dose and dosing frequency for each subject will depend on the subject's body weight. Subjects who will receive treatment every two weeks will receive a loading dose corresponding to a double dose at baseline. Subjects who will receive treatment every 4 weeks will receive a staggered loading dose at baseline and Week 2. After the loading dose, they will continue to receive treatment every 4 weeks. The dose and dosing frequency will be adjusted according to the subject's body weight at weeks 16, 32, 52, 64, 88, 112, 136, 160, and 184. |
|
Экспериментальный: Placebo + TCS for subjects aged 2 to <12 years
Dose and dosing frequency for each subject will depend on the subject's body weight. |
The trial medication will be given under the skin (SC). Dose and dosing frequency for each subject will depend on the subject's body weight. Subjects who will receive treatment every two weeks will receive a loading dose corresponding to a double dose at baseline. Subjects who will receive treatment every 4 weeks will receive a staggered loading dose at baseline and Week 2. After the loading dose, they will continue to receive treatment every 4 weeks. The dose and dosing frequency will be adjusted according to the subject's body weight at weeks 16, 32, 52, 64, 88, 112, 136, 160, and 184. |
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Экспериментальный: Tralokinumab + TCS for subjects aged 6 months to <2 years
Dose and dosing frequency for each subject will depend on the subject's body weight. |
The trial medication will be given under the skin (SC). Dose and dosing frequency for each subject will depend on the subject's body weight. Subjects who will receive treatment every two weeks will receive a loading dose corresponding to a double dose at baseline. Subjects who will receive treatment every 4 weeks will receive a staggered loading dose at baseline and Week 2. After the loading dose, they will continue to receive treatment every 4 weeks. The dose and dosing frequency will be adjusted according to the subject's body weight at weeks 16, 32, 52, 64, 88, 112, 136, 160, and 184. |
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 16
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The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 16
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Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 16
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The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 16
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Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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Наличие антилекарственных антител, возникших во время лечения (да/нет) у субъектов в возрасте от 2 до <12 лет при скрининге.
Временное ограничение: От исходного уровня до 16-й недели
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От исходного уровня до 16-й недели
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Наличие антилекарственных антител, возникших во время лечения (да/нет) у субъектов в возрасте от 6 месяцев до <2 лет при скрининге.
Временное ограничение: От исходного уровня до 16-й недели
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От исходного уровня до 16-й недели
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Использование спасательной терапии (да/нет) у субъектов в возрасте от 2 до <12 лет на момент скрининга.
Временное ограничение: От исходного уровня до 16-й недели
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От исходного уровня до 16-й недели
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Использование экстренной терапии (да/нет) у субъектов в возрасте от 6 месяцев до <2 лет на момент скрининга.
Временное ограничение: От исходного уровня до 16-й недели
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От исходного уровня до 16-й недели
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Процентное изменение пораженной площади поверхности тела (ППТ) у субъектов в возрасте от 2 до <12 лет на момент скрининга.
Временное ограничение: От исходного уровня до 52-й недели
|
От исходного уровня до 52-й недели
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Процентное изменение пораженной площади поверхности тела (ППТ) у субъектов в возрасте от 6 месяцев до <2 лет на момент скрининга.
Временное ограничение: От исходного уровня до 52-й недели
|
От исходного уровня до 52-й недели
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Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 16
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 16
|
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Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 16
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 16
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 16
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 16
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 16
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 16
|
|
Having at least 50% reduction in EASI score in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 16
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 16
|
|
Having at least 50% reduction in EASI score in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 16
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 16
|
|
Percent change in EASI in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 16
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 16
|
|
Percent change in EASI in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 16
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 16
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 16
|
The SCORAD is a validated tool to evaluate the extent and severity of atopic dermatitis. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 16
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 16
|
The SCORAD is a validated tool to evaluate the extent and severity of atopic dermatitis. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 16
|
|
Percent change in affected BSA in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 16
|
BSA is a body surface area. |
From baseline to week 16
|
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Percent change in affected BSA in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 16
|
BSA is a body surface area. |
From baseline to week 16
|
|
Percent change in Children's Dermatology Life Quality Index (CDLQI) for subjects aged 4 to <12 years at screening.
Временное ограничение: From baseline to Week 16
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to Week 16
|
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Reduction in Child Worst Itch numeric rating score (NRS) (weekly average) ≥4 for subjects aged 6 to <12 years at screening.
Временное ограничение: From baseline to Week 16
|
The Child Worst Itch NRS assesses 'worst itch today' and 'worst itch last night' using a numerical rating scale from 0 to 10, where 0 represents 'Not itchy at all' and 10 represents 'Very itchy'. |
From baseline to Week 16
|
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Reduction in Scratch Observer-Reported Outcome (ObsRO) (weekly average) ≥4 for subjects aged 2 to <6 years at screening.
Временное ограничение: From baseline to week 16
|
The Scratch ObsRO NRS assesses 'worst scratching during the past 24 hours' using a numerical rating scale from 0 to 10, where 0 represents 'No scratching' and 10 represents 'Worst scratching possible'. |
From baseline to week 16
|
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Reduction in Scratch Observer-Reported Outcome (ObsRO) (weekly average) ≥4 for subjects aged 6 months to <2 years years at screening.
Временное ограничение: From baseline to week 16
|
The Scratch ObsRO NRS assesses 'worst scratching during the past 24 hours' using a numerical rating scale from 0 to 10, where 0 represents 'No scratching' and 10 represents 'Worst scratching possible'. |
From baseline to week 16
|
|
Reduction of ≥4 in Child Worst Itch NRS (weekly average) for subjects aged 6 to <12 years at screening or Scratch ObsRO (weekly average) for subjects aged 2 to <6 years at screening.
Временное ограничение: From baseline to week 16
|
The Child Worst Itch NRS assesses 'worst itch today' and 'worst itch last night' using a numerical rating scale from 0 to 10, where 0 represents 'Not itchy at all' and 10 represents 'Very itchy'. The Scratch ObsRO NRS assesses 'worst scratching during the past 24 hours' using a numerical rating scale from 0 to 10, where 0 represents 'No scratching' and 10 represents 'Worst scratching possible'. |
From baseline to week 16
|
|
Percent change in Patient-Oriented Eczema Measure (POEM) in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 16
|
The POEM is a validated questionnaire used to assess disease symptoms in atopic eczema patients in both clinical practice and clinical trials. The tool consists of 7 items each addressing a specific symptom (itching, sleep, bleeding, weeping, cracking, flaking, and dryness). Subjects will score how often they have experienced each symptom over the previous week on a 5-point categorical response scale (0 = 'no days'; 1 = '1 to 2 days'; 2 = '3 to 4 days'; 3 = '5 to 6'days; 4 = 'every day'). The total score is the sum of the 7 items (range 0 to 28) and reflects disease-related morbidity; a high score is indicative of a worse disease severity. |
From baseline to week 16
|
|
Percent change in Patient-Oriented Eczema Measure (POEM) in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 16
|
The POEM is a validated questionnaire used to assess disease symptoms in atopic eczema patients in both clinical practice and clinical trials. The tool consists of 7 items each addressing a specific symptom (itching, sleep, bleeding, weeping, cracking, flaking, and dryness). Subjects will score how often they have experienced each symptom over the previous week on a 5-point categorical response scale (0 = 'no days'; 1 = '1 to 2 days'; 2 = '3 to 4 days'; 3 = '5 to 6'days; 4 = 'every day'). The total score is the sum of the 7 items (range 0 to 28) and reflects disease-related morbidity; a high score is indicative of a worse disease severity. |
From baseline to week 16
|
|
Reduction of in Patient-Oriented Eczema Measure (POEM) ≥6 in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 16
|
The POEM is a validated questionnaire used to assess disease symptoms in atopic eczema patients in both clinical practice and clinical trials. The tool consists of 7 items each addressing a specific symptom (itching, sleep, bleeding, weeping, cracking, flaking, and dryness). Subjects will score how often they have experienced each symptom over the previous week on a 5-point categorical response scale (0 = 'no days'; 1 = '1 to 2 days'; 2 = '3 to 4 days'; 3 = '5 to 6'days; 4 = 'every day'). The total score is the sum of the 7 items (range 0 to 28) and reflects disease-related morbidity; a high score is indicative of a worse disease severity. |
From baseline to week 16
|
|
Reduction of in Patient-Oriented Eczema Measure (POEM) ≥6 in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 16
|
The POEM is a validated questionnaire used to assess disease symptoms in atopic eczema patients in both clinical practice and clinical trials. The tool consists of 7 items each addressing a specific symptom (itching, sleep, bleeding, weeping, cracking, flaking, and dryness). Subjects will score how often they have experienced each symptom over the previous week on a 5-point categorical response scale (0 = 'no days'; 1 = '1 to 2 days'; 2 = '3 to 4 days'; 3 = '5 to 6'days; 4 = 'every day'). The total score is the sum of the 7 items (range 0 to 28) and reflects disease-related morbidity; a high score is indicative of a worse disease severity. |
From baseline to week 16
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 16
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 16
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 16
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 16
|
|
Change in Child Worst Itch NRS (weekly average) for subjects aged 6 to <12 years at screening.
Временное ограничение: From baseline to week 16
|
The Scratch ObsRO NRS assesses 'worst scratching during the past 24 hours' using a numerical rating scale from 0 to 10, where 0 represents 'No scratching' and 10 represents 'Worst scratching possible'. |
From baseline to week 16
|
|
Change in Scratch Observer-Reported Outcome (ObsRO) (weekly average) in subjects aged 2 to <6 years at screening.
Временное ограничение: From baseline to week 16
|
The Scratch ObsRO NRS assesses 'worst scratching during the past 24 hours' using a numerical rating scale from 0 to 10, where 0 represents 'No scratching' and 10 represents 'Worst scratching possible'. |
From baseline to week 16
|
|
Change in Scratch Observer-Reported Outcome (ObsRO) (weekly average) in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 16
|
The Scratch ObsRO NRS assesses 'worst scratching during the past 24 hours' using a numerical rating scale from 0 to 10, where 0 represents 'No scratching' and 10 represents 'Worst scratching possible'. |
From baseline to week 16
|
|
Reduction in Children's Dermatology Life Quality Index (CDLQI) ≥6 for subjects aged 4 to <12 years at screening.
Временное ограничение: From baseline to week 16
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 16
|
|
Number of treatment-emergent adverse events (AEs) per subject aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 16
|
An adverse event (AE) is any unexpected medical issue that happens to a person who is taking a medication or participating in a study. It could be a symptom, disease, or abnormal test result, even if it's not necessarily caused by the medication being used. |
From baseline to week 16
|
|
Number of treatment-emergent adverse events (AEs) per subject aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 16
|
An adverse event (AE) is any unexpected medical issue that happens to a person who is taking a medication or participating in a study. It could be a symptom, disease, or abnormal test result, even if it's not necessarily caused by the medication being used. |
From baseline to week 16
|
|
Number of TCS free days in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 16
|
TCS- tropical corticosteroids. |
From baseline to week 16
|
|
Number of TCS free days in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 16
|
TCS- tropical corticosteroids. |
From baseline to week 16
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 52
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 52
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 52
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 52
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 52
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 52
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 52
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 52
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 52
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 52
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 52
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 52
|
|
Percent change in EASI in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 52
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 52
|
|
Percent change in EASI in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 52
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 52
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 52
|
The SCORAD is a validated tool to evaluate the extent and severity of atopic dermatitis. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 52
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 52
|
The SCORAD is a validated tool to evaluate the extent and severity of atopic dermatitis. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 52
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 52
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 52
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 52
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 52
|
|
Percent change in Children's Dermatology Life Quality Index (CDLQI) in subjects aged 4 to <12 years at screening.
Временное ограничение: From baseline to week 52
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 52
|
|
Reduction in Children's Dermatology Life Quality Index (CDLQI) ≥6 for subjects aged 4 to <12 years at screening.
Временное ограничение: From baseline to week 52
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 52
|
|
Reduction of in Patient-Oriented Eczema Measure (POEM) ≥6 in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 52
|
The POEM is a validated questionnaire used to assess disease symptoms in atopic eczema patients in both clinical practice and clinical trials. The tool consists of 7 items each addressing a specific symptom (itching, sleep, bleeding, weeping, cracking, flaking, and dryness). Subjects will score how often they have experienced each symptom over the previous week on a 5-point categorical response scale (0 = 'no days'; 1 = '1 to 2 days'; 2 = '3 to 4 days'; 3 = '5 to 6'days; 4 = 'every day'). The total score is the sum of the 7 items (range 0 to 28) and reflects disease-related morbidity; a high score is indicative of a worse disease severity. |
From baseline to week 52
|
|
Reduction of in Patient-Oriented Eczema Measure (POEM) ≥6 in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 52
|
The POEM is a validated questionnaire used to assess disease symptoms in atopic eczema patients in both clinical practice and clinical trials. The tool consists of 7 items each addressing a specific symptom (itching, sleep, bleeding, weeping, cracking, flaking, and dryness). Subjects will score how often they have experienced each symptom over the previous week on a 5-point categorical response scale (0 = 'no days'; 1 = '1 to 2 days'; 2 = '3 to 4 days'; 3 = '5 to 6'days; 4 = 'every day'). The total score is the sum of the 7 items (range 0 to 28) and reflects disease-related morbidity; a high score is indicative of a worse disease severity. |
From baseline to week 52
|
|
Number of treatment-emergent adverse events (AEs) per subject aged 2 to <12 years at screening.
Временное ограничение: From week 16 to 52
|
An adverse event (AE) is any unexpected medical issue that happens to a person who is taking a medication or participating in a study. It could be a symptom, disease, or abnormal test result, even if it's not necessarily caused by the medication being used. |
From week 16 to 52
|
|
Number of treatment-emergent adverse events (AEs) per subject aged 6 month to <2 years at screening.
Временное ограничение: From week 16 to 52
|
An adverse event (AE) is any unexpected medical issue that happens to a person who is taking a medication or participating in a study. It could be a symptom, disease, or abnormal test result, even if it's not necessarily caused by the medication being used. |
From week 16 to 52
|
|
Presence of treatment-emergent anti-drug antibodies (yes/no) in subjects aged 2 to <12 years at screening.
Временное ограничение: From week 16 to 52
|
It measures whether the developed antibodies in response to the treatment have any effect on the safety and effectiveness of the treatment. |
From week 16 to 52
|
|
Presence of treatment-emergent anti-drug antibodies (yes/no) in subjects aged 6 month to <2 years at screening.
Временное ограничение: From week 16 to 52
|
It measures whether the developed antibodies in response to the treatment have any effect on the safety and effectiveness of the treatment. |
From week 16 to 52
|
|
Number of treatment-emergent adverse events (AEs) per subject aged 2 to <12 years at screening.
Временное ограничение: From week 52 to end of treatment
|
An adverse event (AE) is any unexpected medical issue that happens to a person who is taking a medication or participating in a study. It could be a symptom, disease, or abnormal test result, even if it's not necessarily caused by the medication being used. |
From week 52 to end of treatment
|
|
Number of treatment-emergent adverse events (AEs) per subject aged 6 month to <2 years at screening.
Временное ограничение: From week 52 to end of treatment
|
An adverse event (AE) is any unexpected medical issue that happens to a person who is taking a medication or participating in a study. It could be a symptom, disease, or abnormal test result, even if it's not necessarily caused by the medication being used. |
From week 52 to end of treatment
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 100
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 100
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 100
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 100
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 100
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 100
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 100
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 100
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 100
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 100
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 100
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 100
|
|
Percent change in EASI in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 100
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 100
|
|
Percent change in EASI in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 100
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 100
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 100
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 100
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 100
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 100
|
|
Percent change in Children's Dermatology Life Quality Index (CDLQI) for subjects aged 4 to <12 years at screening.
Временное ограничение: From baseline to week 100
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 100
|
|
Reduction in Children's Dermatology Life Quality Index (CDLQI) ≥ 6 for subjects aged 4 to <12 years at screening.
Временное ограничение: From baseline to week 100
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 100
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 148
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 148
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 148
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 148
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 148
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 148
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 148
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 148
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 148
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 148
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 148
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 148
|
|
Percent change in EASI in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 148
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 148
|
|
Percent change in EASI in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 148
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 148
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 148
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 148
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 148
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 148
|
|
Percent change in Children's Dermatology Life Quality Index (CDLQI) for subjects aged 4 to <12 years at screening.
Временное ограничение: From baseline to week 148
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 148
|
|
Reduction in Children's Dermatology Life Quality Index (CDLQI) ≥ 6 for subjects aged 4 to <12 years at screening.
Временное ограничение: From baseline to week 148
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 148
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 196
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 196
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 196
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 196
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 196
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 196
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 196
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 196
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Временное ограничение: At week 196
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 196
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Временное ограничение: At week 196
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 196
|
|
Percent change in EASI in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 196
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 196
|
|
Percent change in EASI in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 196
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 196
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 2 to <12 years at screening.
Временное ограничение: From baseline to week 196
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 196
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 6 month to <2 years at screening.
Временное ограничение: From baseline to week 196
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 196
|
|
Percent change in Children's Dermatology Life Quality Index (CDLQI) for subjects aged 4 to <12 years at screening.
Временное ограничение: From baseline to week 196
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 196
|
|
Reduction in Children's Dermatology Life Quality Index (CDLQI) ≥ 6 for subjects aged 4 to <12 years at screening.
Временное ограничение: From baseline to week 196
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 196
|
Соавторы и исследователи
Спонсор
Следователи
- Директор по исследованиям: Medical Expert, LEO Pharma
Даты записи исследования
Изучение основных дат
Начало исследования (Действительный)
Первичное завершение (Действительный)
Завершение исследования (Оцененный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Действительный)
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Дополнительные соответствующие термины MeSH
- Генетические заболевания, врожденные
- Заболевания иммунной системы
- Гиперчувствительность, немедленная
- Гиперчувствительность
- Кожные заболевания
- Кожные заболевания, генетические
- Кожные заболевания, экзематозные
- Дерматит
- Врожденные, наследственные и неонатальные заболевания и аномалии
- Заболевания кожи и соединительной ткани
- Дерматит, атопический
- Еда
- Диета, еда и питание
- Физиологические явления
- Еда и напитки
- тралокинумаб
- Меласса
Другие идентификационные номера исследования
- LP0162-1336
- U1111-1285-6559 (Другой идентификатор: World Health Organization (WHO))
- 2023-503630-44-00 (Ктис)
- 2023 (Грант/контракт NIH США)
Планирование данных отдельных участников (IPD)
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Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
продукт, произведенный в США и экспортированный из США.
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .