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临床试验/NCT02998528
NCT02998528已完成3 期

Randomized, OpenLabel, Phase 3 Trial of Nivolumab Plus Ipilimumab or Nivolumab Plus Platinum Doublet Chemotherapy Versus Platinum Doublet Chemotherapy in Early Stage NSCLC

Bristol-Myers Squibb273 个研究点 分布在 1 个国家目标入组 505 人开始时间: 2017年3月4日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
505
试验地点
273
主要终点
Event-Free Survival (EFS)

研究概览

简要总结

The purpose of this neoadjuvant study is to compare nivolumab plus chemotherapy and chemotherapy alone in terms of safety and effectiveness, and to describe nivolumab plus ipilimumab's safety and effectiveness in treating resectable NSCLC.

This study has multiple primary endpoints.

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

  • Early stage IB-IIIA, operable non-small cell lung cancer, confirmed in tissue
  • Lung function capacity capable of tolerating the proposed lung surgery
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1
  • Available tissue of primary lung tumor

排除标准

  • Presence of locally advanced, inoperable or metastatic disease
  • Participants with active, known or suspected autoimmune disease
  • Prior treatment with any drug that targets T cell co-stimulations pathways (such as checkpoint inhibitors)
  • Other protocol defined inclusion/exclusion criteria apply

研究组 & 干预措施

Nivolumab plus platinum doublet chemotherapy

Experimental

Specified dose on specified days

干预措施: Nivolumab (Biological)

Platinum doublet chemotherapy

Active Comparator

Specified dose on specified days

干预措施: Carboplatin (Drug)

Platinum doublet chemotherapy

Active Comparator

Specified dose on specified days

干预措施: Paclitaxel (Drug)

Platinum doublet chemotherapy

Active Comparator

Specified dose on specified days

干预措施: Cisplatin (Drug)

Platinum doublet chemotherapy

Active Comparator

Specified dose on specified days

干预措施: Vinorelbine (Drug)

Platinum doublet chemotherapy

Active Comparator

Specified dose on specified days

干预措施: Gemcitabine (Drug)

Platinum doublet chemotherapy

Active Comparator

Specified dose on specified days

干预措施: Docetaxel (Drug)

Platinum doublet chemotherapy

Active Comparator

Specified dose on specified days

干预措施: Pemetrexed (Drug)

Nivolumab plus platinum doublet chemotherapy

Experimental

Specified dose on specified days

干预措施: Cisplatin (Drug)

Nivolumab plus platinum doublet chemotherapy

Experimental

Specified dose on specified days

干预措施: Gemcitabine (Drug)

Nivolumab plus platinum doublet chemotherapy

Experimental

Specified dose on specified days

干预措施: Pemetrexed (Drug)

Nivolumab plus platinum doublet chemotherapy

Experimental

Specified dose on specified days

干预措施: Carboplatin (Drug)

Nivolumab plus platinum doublet chemotherapy

Experimental

Specified dose on specified days

干预措施: Paclitaxel (Drug)

Nivolumab plus Ipilimumab

Experimental

Specified dose on specified days

干预措施: Nivolumab (Biological)

Nivolumab plus Ipilimumab

Experimental

Specified dose on specified days

干预措施: Ipilimumab (Biological)

结局指标

主要结局

Event-Free Survival (EFS)

时间窗: From randomization to disease progression, reoccurrence, or death due to any cause. (Up to a median of 30 months)

Event-free survival (EFS) is defined as the length of time from randomization to any of the following events: any progression of disease precluding surgery, progression or recurrence disease based on blinded independent central review (BICR) assessment per response evaluation criteria in solid tumors (RECIST) 1.1 after surgery, or death due to any cause. Participants who don't undergo surgery for reason other than progression will be considered to have an event at progression or death. Progression is defined as at least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study. In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of at least 5 mm. (Note: the appearance of one or more new lesions is also considered progression).

Pathologic Complete Response (pCR) Rate

时间窗: From randomization up to a median of 30 months after randomization.

Pathologic complete response (pCR) rate is defined as the number of randomized participants with absence of residual tumor in lung and lymph nodes as evaluated by blinded independent pathological review (BIPR).

次要结局

  • Major Pathologic Response (MPR) Rate(From randomization up to a median of 30 months after randomization.)
  • Overall Survival (OS)(From randomization to the date of death (Up to approximately 93 months))
  • Time to Death or Distant Metastases (TTDM)(From randomization to the first date of distant metastasis or the date of death in the absence of distant metastasis (Up to approximately 84 months))

研究者

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

研究点 (273)

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