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Набира участници Фаза 2 2024-519884-16-00

Ultimate dePletion of autoReactive b cells using Obinutuzumab from sjÖgren's syndrome affected Tissues study- UPROOT study

Фаза 2 – изследване на ефективността и дозировката
Заболявания: Sjögren's syndrome

Спонсор: Radboud universitair medisch centrum Stichting

Налично на: БГ
Обобщение
Trial status: Authorised - Change from baseline in ESSDAI score at Week 12, 24 and 36 (11)., - Proportion of patients achieving ≥3 points reduction from baseline in ESSDAIscore at Week 12, 24 and 36., - Proportion of patients achieving ESSDAI<5 at Week 12, 24 and 36., - Change from baseline in PhGA of disease activity at Week 12, 24 and 36, - Change from baseline in PaGA of disease activity at Week 12, 24 and 36., - Proportion of patients achieving ≥ 1 point or 15% reduction from baseline in ESSPRI at Week 12, 24 and 36 (11)., 1. Change from baseline in STAR, Schirmer’s test, unstimulated whole saliva secretion Depletion of anti-Ro60, anti-Ro52, anti-La and rheumatoid factor B cells in blood, inflamed salivary gland and involved lymph node of patients with SjS at 3 months after initiation of Obinutuzumab compared to sampling before treatment initiation.
Описание
- Change from baseline in ESSDAI score at Week 12, 24 and 36 (11)., - Proportion of patients achieving ≥3 points reduction from baseline in ESSDAIscore at Week 12, 24 and 36., - Proportion of patients achieving ESSDAI<5 at Week 12, 24 and 36., - Change from baseline in PhGA of disease activity at Week 12, 24 and 36, - Change from baseline in PaGA of disease activity at Week 12, 24 and 36., - Proportion of patients achieving ≥ 1 point or 15% reduction from baseline in ESSPRI at Week 12, 24 and 36 (11)., 1. Change from baseline in STAR, Schirmer’s test, unstimulated whole saliva secretion
Кой може да участва
Age group: 18-64 years, 65+ years Gender: Female, Male Target enrollment: 10 participants
Интервенции
Gazyvaro 1,000 mg concentrate for solution for infusion.
Drug
Места на провеждане 1
Нидерландия (1)
Технически детайли
Статус
Набира участници
Фаза
Фаза 2
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Здрави доброволци
Не
Начална дата
11.03.2026
Регистрационен номер
2024-519884-16-00
Източник
euclinicaltrials.eu
Запитване за медицински туризъм

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