LUME-Meso: Double Blind, Randomised, Multicentre, Phase II/III Study of Nintedanib in Combination With Pemetrexed / Cisplatin Followed by Continuing Nintedanib Monotherapy Versus Placebo in Combination With Pemetrexed / Cisplatin Followed by Continuing Placebo Monotherapy for the Treatment of Patients With Unresectable Malignant Pleural Mesothelioma
试验速览
- 阶段
- 2 期
- 状态
- 终止
- 入组人数
- 545
- 试验地点
- 122
- 主要终点
- Progression-Free Survival (PFS)
研究概览
简要总结
This is a phase II/III confirmatory study designed to evaluate the safety and efficacy of nintedanib (BIBF 1120) in combination + (pemetrexed / cisplatin) followed by nintedanib (BIBF 1120) versus placebo + pemetrexed / cisplatin followed by placebo for the treatment of patients with unresectable malignant pleural mesothelioma.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
研究组 & 干预措施
Placebo + pemetrexed/cisplatin
Placebo controlled arm
干预措施: Pemetrexed (Drug)
Placebo + pemetrexed/cisplatin
Placebo controlled arm
干预措施: Cisplatin (Drug)
Placebo + pemetrexed/cisplatin
Placebo controlled arm
干预措施: Placebo (Drug)
Nintedanib 200mg + pemetrexed/cisplatin
Experimental arm
干预措施: Nintedanib (Drug)
Nintedanib 200mg + pemetrexed/cisplatin
Experimental arm
干预措施: Cisplatin (Drug)
Nintedanib 200mg + pemetrexed/cisplatin
Experimental arm
干预措施: Pemetrexed (Drug)
结局指标
主要结局
Progression-Free Survival (PFS)
时间窗: From randomization until the earliest of disease progression, death or (Phase II: cut-off date of 4-March-2016; up to 889 days) (Phase III: cut-off date of 16-March-2018; up to 31 months)
This outcome measure presents progression-free survival. Disease progression was defined according to the modified Response Evaluation Criteria in Solid Tumours (RECIST) criteria. Progression-free survival time was calculated as the duration from the date of randomization to the date of disease progression or death, whichever occurred first. For patients with known date of progression (or death): PFS (days) = min (date of progression, date of death) - date of randomization + 1 day. For patients without progression or death, PFS was censored at the last imaging date that showed no disease progression: PFS (days, censored) = date of last imaging showing no progression - date randomization + 1 day.
次要结局
- Overall Survival (OS)(From randomization until the earliest of disease progression, death or (Phase II: cut-off date of 4-March-2016; up to 889 days) (Phase III: cut-off date of 16-March-2018; up to 31 months))
- Objective Response According to Modified RECIST- Investigator Assessment(Tumour imaging was to be performed every 6 weeks until disease progression, death or start of subsequent anti-cancer therapy, whichever occurred earlier; up to 54 months)
- Disease Control According to Modified RECIST- Investigator Assessment(Tumour imaging was to be performed every 6 weeks until disease progression, death or start of subsequent anti-cancer therapy, whichever occurred earlier; up to 54 months)
