BENITIONSClinical Trial Intelligence

An Open-label, Phase 2 Study of ACP-196 (Acalabrutinib) in Subjects With Mantle Cell Lymphoma

2期 进行中(已停止招募) NCT02213926

适应症Mantle Cell Lymphoma
分期2期
申办方Acerta Pharma BV
状态进行中(已停止招募)
受试者人数124 人
干预(药物)ACP-196 (acalabrutinib)
开始日期2015年3月2日
完成日期2020年12月4日
结果公布日2018年10月19日

摘要

The purpose of this study is to characterize the safety and efficacy profile of ACP-196 (acalabrutinib) in subjects with relapsed or refractory Mantle Cell Lymphoma (MCL).

Overall Response Rate (ORR) of ACP-196 (Acalabrutinib) in Subjects With Previously Treated MCL.

From the date of the first dose until 30 days after the last dose of the study drug or start of a new anti-cancer treatment, whichever came first, assessed up to approximately 4 year and 10 months. 1 cycle =28 days · Participants

ACP-196 (Acalabrutinib)59 Participants
ACP-196 (Acalabrutinib)42 Participants
ACP-196 (Acalabrutinib)10 Participants
ACP-196 (Acalabrutinib)10 Participants
ACP-196 (Acalabrutinib)3 Participants

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

同一适应症的其他试验

全部试验

本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。