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CLICK-MS 和 MASTER-2 四期临床试验设计:克拉屈滨片治疗控制不佳的复发型多发性硬化症。

CLICK-MS and MASTER-2 Phase IV trial design: cladribine tablets in suboptimally controlled relapsing multiple sclerosis.

机构信息

Advanced Neurology of Colorado, University of Colorado, Fort Collins, CO 80528, USA.

Elliot Lewis Center for Multiple Sclerosis Care, Wellesley, MA 02481, USA.

出版信息

Neurodegener Dis Manag. 2021 Apr;11(2):99-111. doi: 10.2217/nmt-2020-0059. Epub 2021 Feb 1.

Abstract

Cladribine tablets 10 mg (3.5 mg/kg cumulative dose over 2 years) are approved for the treatment of relapsing forms of multiple sclerosis (MS), including relapsing-remitting MS and active secondary progressive MS. However, real-world data on cladribine tablets are limited. CLICK-MS and MASTER-2 are single arm, observational, 30-month, Phase IV studies in the US evaluating the effectiveness and safety of cladribine tablets 3.5 mg/kg in patients with relapsing-remitting MS or active secondary progressive MS who had suboptimal response to prior injectable (CLICK-MS), or infusion/oral (MASTER-2) disease-modifying therapy. The primary end point is 24-month annualized relapse rate. Key secondary end points include patient-reported outcomes on quality of life measures, treatment adherence and adverse events. Studies began in 2019 and are expected to be completed in 2023. • CLICK-MS: NCT03933215 (ClinicalTrials.gov) ; adribine tablets: observational evaluation of effectveness and patient-reported outcomes in suboptimally ontrolled patients previously taing injectable disease-modifying drugs for relapsing forms of ultiple clerosis • MASTER-2: NCT03933202 (ClinicalTrials.gov) ; Cladribine tablets: observational evaluation of effectiveness and patient-reported outcomes in suboptilly controlled patient previously aking oral or infusion disase-modifying dugs for relapsing forms of multiple sclerosis.

摘要

氯法拉滨片剂 10mg(2 年内累积剂量 3.5mg/kg)获批用于治疗多发性硬化症(MS)的复发型,包括复发缓解型 MS 和活动性继发进展型 MS。然而,氯法拉滨片剂的真实世界数据有限。CLICKS 和 MASTER-2 是美国的两项单臂、观察性、30 个月、IV 期研究,评估了氯法拉滨片剂 3.5mg/kg 在先前接受过不理想的注射(CLICKS)或输注/口服(MASTER-2)疾病修正治疗的复发缓解型 MS 或活动性继发进展型 MS 患者中的有效性和安全性。主要终点是 24 个月的年化复发率。关键次要终点包括生活质量措施的患者报告结果、治疗依从性和不良事件。研究于 2019 年开始,预计将于 2023 年完成。

  • CLICKS-MS:NCT03933215(ClinicalTrials.gov);氯法拉滨片剂:先前接受过注射用疾病修正药物治疗的复发型多发性硬化症患者的有效性和患者报告结果的观察性评估

  • MASTER-2:NCT03933202(ClinicalTrials.gov);氯法拉滨片剂:先前接受过口服或输注用疾病修正药物治疗的复发型多发性硬化症患者的有效性和患者报告结果的观察性评估

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