- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT07919899
Pharmacokinetics, Immunogenicity and Safety of Subcutaneous Dupilumab and Berahyaluronidase Alfa (ALT-B4) Coformulation (EXTENSA)
A Randomized, Open-label, Multiple-dose Phase 3 Study to Evaluate Pharmacokinetics, Immunogenicity and Safety of Subcutaneous Dupilumab and Berahyaluronidase Alfa (ALT-B4) Coformulation Compared to the Approved Subcutaneous Dupilumab Formulation in Adults and Adolescents With Moderate-to-severe Atopic Dermatitis
This is a Phase 3, open label, randomized, parallel-group, 2-arm study. The purpose of this study is to measure PK, immunogenicity, safety and, tolerability of dupilumab hyaluronidase coformulation compared with dupilumab approved formulation in male or female participants with moderate-to-severe atopic dermatitis (AD) aged ≥12 years of age. Study details as follows:
- The study duration includes screening period up to 4 weeks + treatment period of 20 weeks (± 3 days) and follow-up of 12 weeks (± 7 days).
- The number of on-site visits will be 10 and one phone contact will be scheduled (during the follow-up period).
Обзор исследования
Статус
Условия
Вмешательство/лечение
Тип исследования
Регистрация (Оцененный)
Фаза
- Фаза 3
Контакты и местонахождение
Контакты исследования
- Имя: Trial Transparency email recommended (Toll free for US & Canada)
- Номер телефона: option 6 800-633-1610
- Электронная почта: Contact-US@sanofi.com
Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
Принимает здоровых добровольцев
Полы, имеющие право на обучение
Описание
Inclusion Criteria:
-
Participant must be ≥12 years of age at the time of signing the informed consent.
-
Participants with chronic AD, (according to American Academy of Dermatology Consensus Criteria, that has been present for at least 12 months before the screening visit.
-
Participants with ≥10% body surface area (BSA) of AD involvement at the screening and baseline visits.
-
Participant's AD must be graded as Eczema Area and Severity Index (EASI) score ≥16 at the screening and baseline visits.
-
Validated Investigator Global Assessment for Atopic Dermatitis (v-IGA) ≥3 at the screening and baseline visits.
-
Worst-Itch Numerical Rating Scale (WI-NRS) weekly average score ≥4 in the 7 days before randomization.
-
Documented recent history (within 6 months before the screening visit) of inadequate response* to treatment with topical medications or for whom topical treatments are otherwise medically inadvisable (eg, because of important side effects or safety risks).
*Inadequate response to topical therapy is defined as persistent moderate-to-severe AD (EASI ≥16, vIGA-AD ≥3, BSA ≥10%) despite ≥4 weeks of optimized topical anti-inflammatory treatment (medium/high potency corticosteroids ± calcineurin inhibitors), or documented intolerance/contraindication to such therapies.
-
For adolescents (≥12 and <18 years old) only, body weight ≥60 kg.
Exclusion Criteria:
- Any history or presence of severe concomitant illness(es) that, in the Investigator's judgment, would adversely affect the participant's participation in the study. Examples include, but are not limited to participants with short life expectancy, participants with uncontrolled diabetes (hemoglobin A1c ≥9%), participants with cardiovascular conditions (e.g, cardiomyopathy, thromboembolism, Class III or IV cardiac failure according to the New York Heart Association classification), severe hematological conditions (e.g. hyperviscosity), severe renal conditions (e.g, participants on dialysis), hepato-biliary conditions (e.g, Child-Pugh class B or C), neurological conditions (e.g, demyelinating diseases), active major autoimmune diseases (e.g, lupus, inflammatory bowel disease, rheumatoid arthritis, etc), other severe endocrinological, gastrointestinal, metabolic, pulmonary, or lymphatic diseases. The specific justification for participants excluded under this criterion will be noted in study documents (chart notes, case report forms [CRF], etc).
- Active chronic or acute infection requiring treatment with systemic antibiotics, antivirals, antiparasitics, antiprotozoals, or antifungals within 2 weeks before the baseline visit, or superficial skin infections within 1 week before the baseline visit. NOTE: participants may be rescreened after infection resolves.
- Known or suspected history of immunosuppression, including history of invasive opportunistic infections (eg, tuberculosis [TB], histoplasmosis, listeriosis, coccidioidomycosis, pneumocystosis, aspergillosis) despite infection resolution: or unusually frequent, recurrent, or prolonged infections, suggesting immunocompromised status per Investigator judgment.
- Presence of any skin comorbidities other than AD that, in the opinion of the Investigator, may interfere with the assessment of the study outcomes. For example: scabies, insect bite, folliculitis, lymphomatoid papulosis, chronic actinic dermatitis, dermatitis herpetiformis, sporotrichosis, bullous disease, or others.
- History of malignancy within 5 years before the screening visit, except completely treated in situ carcinoma of the cervix, completely treated and resolved non-metastatic squamous or basal cell carcinoma of the skin.
- Diagnosed with, suspected of, or at high risk for endoparasitic infection, and/or use of antiparasitic drugs within 2 weeks before Screening (Visit 1) or during the Screening period.
- Previously treated with marketed dupilumab or having received dupilumab in a prior dupilumab clinical study.
The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Экспериментальный: Dupilumab coformulated with berahyaluronidase alfa
dupilumab coformulated with berahyaluronidase alfa SC injection as per protocol |
Pharmaceutical form: solution for injection Route of administration: SC injection
Другие имена:
|
|
Активный компаратор: Dupilumab approved formulation
Approved dupilumab SC injection as per protocol |
Pharmaceutical form: solution for injection Route of administration: SC injection
Другие имена:
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Ctrough,ss at Week 20
Временное ограничение: Week 20
|
Concentration observed before treatment administration during repeated dosing at steady state (SS). |
Week 20
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
AUC0-4 weeks,ss
Временное ограничение: Week 0 through Week 4
|
Area under curve from time point 0 to 28 days at steady state |
Week 0 through Week 4
|
|
Cmax,ss
Временное ограничение: Week 20
|
Maximum observed concentration during repeated dosing at steady state. |
Week 20
|
|
Incidence of TEAEs, TE-AESIs, TE-SAEs, and TEAEs leading to permanent treatment discontinuation in the treatment-emergent period
Временное ограничение: Week 0 up to week 32
|
TEAEs: treatment-emergent adverse events TE-AESIs: treatment-emergent adverse events of special interest TE-SAE: treatment-emergent serious adverse events |
Week 0 up to week 32
|
|
Incidence of potentially clinically significant abnormalities in laboratory test, vital signs, and ECGs abnormalities in the treatment-emergent period
Временное ограничение: Week 0 up to week 32
|
Week 0 up to week 32
|
|
|
Incidence of treatment-emergent anti-drug antibody (ADA) to dupilumab through Week 20
Временное ограничение: Week 0 up to week 20
|
Week 0 up to week 20
|
|
|
Incidence of treatment-emergent ADA to ALT-B4 through Week 20
Временное ограничение: Week 0 up to week 20
|
Week 0 up to week 20
|
Соавторы и исследователи
Спонсор
Соавторы
Даты записи исследования
Изучение основных дат
Начало исследования (Оцененный)
Первичное завершение (Оцененный)
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
- судурист
Другие идентификационные номера исследования
- EFC20385
- 2026-526619-13 (Идентификатор реестра: CTIS)
- U1111-1333-0202 (Идентификатор реестра: ICTRP)
Планирование данных отдельных участников (IPD)
Планируете делиться данными об отдельных участниках (IPD)?
Описание плана IPD
Qualified researchers may request access to patient level data and related study documents including the clinical study report, study protocol with any amendments, blank case report form, statistical analysis plan, and dataset specifications. Patient level data will be anonymized and study documents will be redacted to protect the privacy of trial participants. Further details on Sanofi's data sharing criteria, eligible studies, and process for requesting access can be found at: https://vivli.org
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.
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. .