跳至主要内容
临床试验/NCT01907100
NCT01907100终止2 期

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

Boehringer Ingelheim122 个研究点 分布在 12 个国家目标入组 545 人开始时间: 2013年9月19日最近更新:
适应症
干预措施
相关药物

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

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 Comparator

Placebo controlled arm

干预措施: Pemetrexed (Drug)

Placebo + pemetrexed/cisplatin

Placebo Comparator

Placebo controlled arm

干预措施: Cisplatin (Drug)

Placebo + pemetrexed/cisplatin

Placebo Comparator

Placebo controlled arm

干预措施: Placebo (Drug)

Nintedanib 200mg + pemetrexed/cisplatin

Experimental

Experimental arm

干预措施: Nintedanib (Drug)

Nintedanib 200mg + pemetrexed/cisplatin

Experimental

Experimental arm

干预措施: Cisplatin (Drug)

Nintedanib 200mg + pemetrexed/cisplatin

Experimental

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)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (122)

Loading locations...

相似试验