BENITIONSClinical Trial Intelligence

A Study to Evaluate the Efficacy and Safety of CAEL-101 in Patients With Mayo Stage IIIb AL Amyloidosis (CARES)

3期 进行中(已停止招募) NCT04504825

适应症AL Amyloidosis
分期3期
申办方Alexion Pharmaceuticals, Inc.
状态进行中(已停止招募)
受试者人数125 人
干预(药物)CAEL-101, cyclophosphamide, bortezomib, and Dexamethasone (CyBorD) regimen
开始日期2020年8月25日
完成日期2025年5月10日
结果公布日2026年7月2日

摘要

AL (or light chain) amyloidosis begins in the bone marrow where abnormal proteins misfold and create free light chains that cannot be broken down. These free light chains bind together to form amyloid fibrils that build up in the extracellular space of organs, affecting the kidneys, heart, liver, spleen, nervous system and digestive tract. The primary purpose of this study is to determine whether CAEL-101, a monoclonal antibody that removes AL amyloid deposits from tissues and organs, improves overall survival, reduces cardiovascular related hospitalizations and it is safe and well tolerated in patients with stage IIIb AL amyloidosis.

A Hierarchical Combination of Time to All-cause Mortality and Frequency of Cardiovascular Hospitalizations (CVHs) Analyzed by Win Ratio

Day 1 through end of the participant's PETP (Participants were enrolled on a rolling basis. Therefore, the primary analysis for the study was conducted 18-47 months after the study randomization.) · win ratio

Combined CAEL-101 + Plasma Cell Dyscrasia Treatment and Placebo + Plasma Cell Dyscrasia Treatment0.95 win ratio
Combined CAEL-101 + Plasma Cell Dyscrasia Treatment and Placebo + Plasma Cell Dyscrasia Treatment1.57 win ratio
Combined CAEL-101 + Plasma Cell Dyscrasia Treatment and Placebo + Plasma Cell Dyscrasia Treatment0.71 win ratio
p-value0.777

Number of Participants With Treatment-emergent Adverse Events (TEAEs)

Day 1 through end of the participant's PETP (Participants were enrolled on a rolling basis. Therefore, the primary analysis for the study was conducted 18-47 months after the study randomization.) · Participants

CAEL-101 + Plasma Cell Dyscrasia Treatment84 Participants
Placebo + Plasma Cell Dyscrasia Treatment40 Participants
CAEL-101 + Plasma Cell Dyscrasia Treatment25 Participants
Placebo + Plasma Cell Dyscrasia Treatment6 Participants
CAEL-101 + Plasma Cell Dyscrasia Treatment57 Participants
Placebo + Plasma Cell Dyscrasia Treatment34 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。