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Набира участници Фаза 1 NCT06333951

Anvumetostat Alone or in Combination With Other Therapies in Subjects With Advanced Thoracic Tumors With Homozygous MTAP-deletion (Master Protocol) (MTAPESTRY 104).

Фаза 1 – тестване на безопасността при малка група хора
Заболявания: Thoracic Tumors Non-small Cell Lung Cancer

Спонсор: Amgen

Налично на: БГ
Обобщение
The study aims to determine maximum tolerated dose (MTD) or recommended combination dose of the MTA-cooperative PRMT5 inhibitor Anvumetostat administered in combination with other therapies in adult participants with metastatic or locally advanced methylthioadenosine phosphorylase (MTAP)-deleted thoracic tumors. The study also aims to determine the safety profile of Anvumetostat administered in combination with other therapies in adult participants with metastatic or locally advanced MTAP-deleted thoracic tumors.
Кой може да участва
Inclusion Criteria Subprotocol A, B, and C * Age ≥ 18 years (or ≥ legal age within the country if it is older than 18 years). * Tumor tissue (formalin-fixed, paraffin-embedded sample) or an archival block must be available. Participants without archived tumor tissue available may be allowed to enroll by undergoing tumor biopsy before Anvumetostat dosing. * Homozygous MTAP-deletion * Able to swallow and retain PO administered study treatment. * Disease measurable as defined by RECIST v1.1. Subprotocol A - Histologically or cytologically confirmed diagnosis of NSCLC. Arm A (Anvumetostat + carboplatin + paclitaxel + pembrolizumab): \- Predominantly squamous histology. Arm B (Anvumetostat + carboplatin + pemetrexed + pembrolizumab): \- Predominantly non-squamous histology. Arm C (Anvumetostat + pembrolizumab): \- PD-L1 positive. Subprotocol B - Histologically confirmed NSCLC with homozygous MTAP-deletion and KRAS p.G12C mutation. Subprotocol C * Histologically or cytologically confirmed diagnosis of NSCLC with brain metastases. * Brain lesion meeting RANO-BM criteria for measurable disease. Exclusion Criteria Subprotocol A, B, and C * Cardiovascular and pulmonary exclusion criteria as defined in the protocol. * Gastrointestinal tract disease causing the inability to take PO medication, malabsorption syndrome, requirement for IV alimentation, gastric/jejunal tube feeds, uncontrolled inflammatory gastrointestinal disease (eg, Crohn's disease, ulcerative colitis). * History of solid organ transplant. * Major surgery within 28 days of first dose of Anvumetostat. * Prior treatment with a MAT2A inhibitor or a PRMT5 inhibitor. * Radiation therapy within 28 days of first dose. Subprotocol A \- Autoimmune disease or immunodeficiency disease as defined in the protocol'
Места на провеждане 19
Argentina (1)
Instituto Argentino de Diagnóstico y Tratamiento
Ciudad Automona de Buenos Aires , Buenos Aires
Австралия (1)
Orange Health Service
Orange , New South Wales
Белгия (1)
Centre Hospitalier Universitaire de Liege - Sart Tilman
Liège
Бразилия (1)
Oncosite Centro de Pesquisa Clinica Em Oncologia Ltda
Ijuí , Rio Grande do Sul
Канада (1)
Princess Margaret Cancer Centre
Toronto , Ontario
Китай (1)
Mengchao Hepatobiliary Hospital of Fujian Medical University
Fuzhou , Fujian
Франция (1)
Institut Bergonie
Bordeaux
Германия (1)
Universitaetsklinikum Essen
Essen
Гърция (1)
Alexandra Hospital
Athens
Hong Kong (1)
Queen Mary Hospital, The University of Hong Kong
Hong Kong
Италия (1)
Fondazione IRCCS Istituto Nazionale dei Tumori
Alessandria
Япония (1)
Aichi Cancer Center
Nagoya , Aichi-ken
Нидерландия (1)
Radboud Universitair Medisch Centrum
Nijmegen
Полша (1)
Uniwersyteckie Centrum Kliniczne
Gdansk
Южна Корея (1)
Seoul National University Hospital
Seoul
Испания (1)
Hospital Universitari Vall d Hebron
Barcelona , Catalonia
Taiwan (1)
National Cheng Kung University Hospital
Tainan
Турция (1)
Adana Sehir Egitim ve Arastirma Hastanesi
Adana
САЩ (1)
Comprehensive Blood and Cancer Center
Bakersfield , California
Технически детайли
Статус
Набира участници
Фаза
Фаза 1
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Максимална възраст
100 Years
Здрави доброволци
Не
Начална дата
17.09.2024
Крайна дата
27.10.2031
Регистрационен номер
NCT06333951
Източник
anzctr
Запитване за медицински туризъм

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