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临床试验/NCT02750514
NCT02750514终止2 期

A Phase 2, Fast Real Time Assessment of Combination Therapies in Immuno-Oncology Study in Subjects With Advanced Non-Small Cell Lung Cancer (FRACTION-Lung)

Bristol-Myers Squibb38 个研究点 分布在 3 个国家目标入组 295 人开始时间: 2016年5月9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
发起方
入组人数
295
试验地点
38
主要终点
Objective Response Rate (ORR)

研究概览

简要总结

The purpose of this study is to determine whether Nivolumab, in combination with other therapies, is effective in patients with advanced Non-Small Cell lung cancer

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
None

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

  • Advanced Non Small Cell Lung Cancer (NSCLC)
  • Eastern Cooperative Oncology Group (ECOG) Performance status of ≤ 1
  • Life expectancy of at least 3 months from most recent chemotherapy or immunotherapy treatment
  • Must have at least 1 lesion with measurable disease

排除标准

  • Subjects with certain mutations that have not been treated with a targeted therapy prior to enrollment
  • Subjects who need daily oxygen therapy
  • People with autoimmune disease
  • Other protocol defined inclusion/exclusion criteria could apply

研究组 & 干预措施

Nivolumab & Relatlimab

Experimental

Nivolumab in combination with Relatlimab

干预措施: Relatlimab (Biological)

Nivolumab

Active Comparator

Nivolumab Monotherapy - Arm associated with this intervention is closed. Nivolumab is no longer given as an active comparator

干预措施: Nivolumab (Biological)

Nivolumab & Dasatinib

Experimental

Nivolumab in combination with Dasatinib

干预措施: Nivolumab (Biological)

Nivolumab & Dasatinib

Experimental

Nivolumab in combination with Dasatinib

干预措施: Dasatinib (Drug)

Nivolumab & Relatlimab

Experimental

Nivolumab in combination with Relatlimab

干预措施: Nivolumab (Biological)

Nivolumab & Ipilimumab

Experimental

Nivolumab in combination with Ipilimumab

干预措施: Nivolumab (Biological)

Nivolumab & Ipilimumab

Experimental

Nivolumab in combination with Ipilimumab

干预措施: Ipilimumab (Biological)

Nivolumab & BMS-986205

Experimental

Nivolumab in combination with BMS- 986205

干预措施: Nivolumab (Biological)

Nivolumab & BMS-986205

Experimental

Nivolumab in combination with BMS- 986205

干预措施: BMS-986205 (Drug)

结局指标

主要结局

Objective Response Rate (ORR)

时间窗: From first dose to 2 years following last dose (up to 30 months)

ORR is defined as the percentage of participants whose confirmed best overall response (BOR) is either a complete response (CR) or partial response (PR). BOR was assessed by investigator per RECIST1.1. Results are presented by study track. Track 1 = participants naive for prior immuno-oncology (IO) therapy and PD-L1 positive Track 2 = participants naive for prior immuno-oncology (IO) therapy and PD-L1 negative Track 3 = participants with prior anti-PD-1/PD-L1 therapy Track 4 = participants naive for prior anti-PD-1/PD-L1 therapy (established upon enrollment closure of tracks 1,2 and 3) Track 5 = participants with prior anti-PD-1/PD-L1 therapy (established upon enrollment closure of tracks 1,2 and 3). Results for each study track are presented only for treatment groups who received a treatment in that specific track.

Duration of Response (DOR)

时间窗: From first dose to 2 years following last dose (up to 30 months)

DOR, computed for all treated participants with a confirmed BOR of CR or PR, is defined as the time between the date of first response and the date of first documented disease progression (as determined by RECIST 1.1) or death due to any cause. Results are presented by study track. Track 1 = participants naive for prior immuno-oncology (IO) therapy and PD-L1 positive Track 2 = participants naive for prior immuno-oncology (IO) therapy and PD-L1 negative Track 3 = participants with prior anti-PD-1/PD-L1 therapy Track 4 = participants naive for prior anti-PD-1/PD-L1 therapy (established upon enrollment closure of tracks 1,2 and 3) Track 5 = participants with prior anti-PD-1/PD-L1 therapy (established upon enrollment closure of tracks 1,2 and 3). Results for each study track are presented only for treatment groups who received a treatment in that specific track.

Progression Free Survival Rate (PFSR) at 24 Weeks

时间窗: From first dose to 24 weeks after first dose

The PFSR at 24 weeks is defined as the proportion of treated participants remaining progression free and surviving at 24 weeks since the first dosing date. Results are presented by study track. Track 1 = participants naive for prior immuno-oncology (IO) therapy and PD-L1 positive (\>=1%) Track 2 = participants naive for prior immuno-oncology (IO) therapy and PD-L1 negative (\<1%) Track 3 = participants with prior anti-PD-1/PD-L1 therapy Track 4 = participants naive for prior anti-PD-1/PD-L1 therapy (established upon enrollment closure of tracks 1,2 and 3) Track 5 = participants with prior anti-PD-1/PD-L1 therapy (established upon enrollment closure of tracks 1,2 and 3). Results for each study track are presented only for treatment groups who received a treatment in that specific track.

次要结局

  • Number of Participants Experiencing Laboratory Abnormalities in Hepatic Tests(From first dose to 100 days following last dose (approximately 9 months))
  • Percentage of Participants Experiencing Death(From first dose to up to 45 months following first dose)
  • Number of Participants Experiencing Laboratory Abnormalities in Thyroid Tests(From first dose to 100 days following last dose (approximately 9 months))
  • Percentage of Participants Experiencing Serious Adverse Events (SAEs)(From first dose to 100 days following last dose)
  • Percentage of Participants Experiencing Adverse Events (AEs) Leading to Discontinuation(From first dose to 100 days following last dose)
  • Percentage of Participants Experiencing Adverse Events (AEs)(From first dose to 100 days following last dose)

研究者

发起方
Bristol-Myers Squibb
申办方类型
Industry
责任方
Sponsor

研究点 (38)

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