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Набира участници NCT07099443

Determinants of the Response to BTK Degraders (BTKd) in Chronic Lymphocytic Leukemia

Заболявания: Chronic Lymphocytic Leukemia BTK Degraders

Спонсор: Nantes University Hospital

Налично на: БГ
Обобщение
The aim of the REBELLE cohort - bio-collection is to collect samples from patients with Chronic Lymphocytic Leukemia candidates or those exposed to BTK degraders to evaluate the mechanisms of resistance to these new molecules. To do this, an additional blood or bone marrow sample to those planned in the context of patient care or a residual lymph node biopsy sample will be collected after signing consent.
Описание
Chronic Lymphocytic Leukemia (CLL) is a malignant hematological disease of B cells, primarily observed in older adults. Although it is classified among indolent hematological malignancies, CLL exhibits significant heterogeneity, both in terms of its biological characteristics and its disease progression and the therapeutic strategies employed. In patients requiring treatment, the disease can relapse. Until recently, immunochemotherapy remained the standard treatment for this disease, but the last decade has seen the emergence of oral targeted therapies, such as Bruton's tyrosine kinase inhibitors (BKT1s) and BCL-2 inhibitors (BCL-2 inhibitors), which have profoundly altered patient prognosis. While the introduction of these two classes of drugs has led to improved prognosis, a rare but significant subgroup of patients, known as "double refractory," has emerged. These patients, exposed to both BKT and BCL-2 inhibitors and who have become refractory to both treatments, have a poor prognosis. To overcome this problem of resistance, molecules targeting the degradation of the BTK protein (BTKd) are currently under development. The main investigator propose the creation of a cohort and a biobank of samples from CLL patients who are candidates for or have been exposed to BTKd, in order to study the mechanisms of response and resistance to these molecules.
Кой може да участва
Inclusion Criteria: * Patient with CLL candidates ou exposed to BTKd * Patient who has provided informed consent to participate in the study. * Patient covered by a social security health insurance plan Exclusion Criteria: * Minor patients. * Adults under guardianship. * Protected persons.
Интервенции
Non-Interventional Sample Collection and Analysis
OTHER
Места на провеждане 14
Франция (14)
CHU de Angers
Angers
NOT_YET_RECRUITING
CHU de Bordeaux
Bordeaux
NOT_YET_RECRUITING
Institut Bergonié
Bordeaux
NOT_YET_RECRUITING
CHU de Clermont-Ferrand
Clermont-Ferrand
NOT_YET_RECRUITING
CHD Vendée
La Roche-sur-Yon
NOT_YET_RECRUITING
Centre Léon Bernard
Lyon
NOT_YET_RECRUITING
Institut Paoli-Calmettes (Marseille)
Marseille
NOT_YET_RECRUITING
CHU de Montpellier
Montpellier
NOT_YET_RECRUITING
Emmanuelle Tchernonog
CH Régional Universitaire de Nancy
Nancy
NOT_YET_RECRUITING
University Hospital
Nantes
Hôpital Avicenne (AP-HP)
Paris
NOT_YET_RECRUITING
Hôpital Universitaire Pitié Salpêtrière de Paris
Paris
NOT_YET_RECRUITING
Damien Roos Weil
CHU de Poitiers
Poitiers
NOT_YET_RECRUITING
Centre Henri-Becquerel de Rouen
Rouen
NOT_YET_RECRUITING
Технически детайли
Статус
Набира участници
Вид изследване
OBSERVATIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Здрави доброволци
Не
Начална дата
09.10.2025
Крайна дата
15.09.2039
Регистрационен номер
NCT07099443
Източник
clinicaltrials.gov
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