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NCT03692442

Evaluation of Efficacy and Toxicity of Nivolumab Monotherapy for Advanced Non-small Cell Lung Cancer After First-line Treatment Failure Based on Second-generation Sequencing and Liquid Chip Platform

Status unknown Last updated 2 October 2018
What this trial tests

trial in Lung Cancer Non-small Cell Stage IV in 80 participants. Status unknown.

Timeline
1 May 2018
Primary endpoint
31 January 2019
31 March 2019

Quick facts

Lead sponsorGuangzhou Institute of Respiratory Disease
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment80
Start date1 May 2018
Primary completion31 January 2019
Estimated completion31 March 2019
Sites1 location across China

Conditions studied

Sponsor

Guangzhou Institute of Respiratory Disease

Who can join

Adults 18 to 65, any sex, with Lung Cancer Non-small Cell Stage IV. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In order to understand the efficacy and side effects of lung cancer immunotherapy, at least 30 patients with lung cancer who were treated with immunotherapy were enrolled. The second-generation sequencing technology and liquid phase factor platform were used for detection, and clinical imaging and other evaluation methods were used to explore the immunotherapy efficacy and side effects affecting lung cancer。

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Resistance to PD-L1/PD-1 Blockade Immunotherapy. A Tumor-Intrinsic or Tumor-Extrinsic Phenomenon?
    Chocarro de Erauso L, Zuazo M, Arasanz H, Bocanegra A, et al · · 2020 · cited 58× · PMID 32317979 · DOI 10.3389/fphar.2020.00441

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Trials by the same sponsor.

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