A Study of Participants in China With Non-Small-Cell Lung Cancer That is Unable to be Treated With Surgery

  • Cancer
  • Lung Cancer
  • Non Small Cell Lung Carcinoma
Please note that the recruitment status of the trial at your site may differ from the overall study status because some study sites may recruit earlier than others.
Trial Status:

Recruiting

This trial runs in
Cities
  • bei-jing-shi
  • Chengdu
  • Harbin
  • Jinan
  • nan-jing-shi
  • nan-ning-shi
  • xi-an-shi
  • zheng-zhou-shi
Trial Identifier:

NCT05872763 ML44633

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      The source of the below information is public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc.. It has been summarised and edited into simpler language. For more information about this clinical trial see the For Expert tab on the specific ForPatients page or follow these links to https://clinicaltrials.gov and/or https://euclinicaltrials.eu and/or https://www.isrctn.com.

      The below information is taken directly from public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc., and has not been edited.

      Results Disclaimer

      Trial Summary

      This is a multicenter, observational cohort study in China with both primary prospective data collection and retrospective collection of prior treatment information from medical records, which enrolls and follows patients who are newly diagnosed with unresectable stage IIIB/IIIC/IV Non-Small-Cell Lung Cancer (NSCLC) in the selected sites. This study aims to describe the clinical practice and long-term survival benefits of patients newly diagnosed with unresectable stage IIIB/IIIC/IV NSCLC. The study also seeks to explore the condition of biomarker tests utilization, and to assess potential economic impact on patients in the real world. The safety related events will also be summarized in this study.

      Hoffmann-La Roche Sponsor
      N/A Phase
      NCT05872763, ML44633 Trial Identifier
      Carcinoma, Non-Small-Cell Lung Condition
      Official Title

      An Observational Cohort Study of Patients With Newly Diagnosed Unresectable Stage IIIB, IIIC, or IV Non-Small-Cell Lung Cancer (NSCLC) in China

      Eligibility Criteria

      All Gender
      All Ages Age
      No Healthy Volunteers
      Inclusion Criteria

      Cohort 1:

      • Participants who have diagnosed with unresectable stage IIIB/IIIC/IV NSCLC
      • Participants who have been diagnosed six months before the start of the study were required to have two complete tumor assessments within at least 6 months intervals after the diagnosis
      • Participants who were newly diagnosed within six months before the start of the study were required to have complete baseline information (see section 6.4.1)
      • Participants who have received standard first-line treatment defined by guideline CSCO (https://www.csco.org.cn/cn/index.aspx) and NCCN (https://www.nccn.org/)

      Cohort 2:

      • Participants who are newly diagnosed with unresectable Stage IIIB/IIIC/IV NSCLC after the start of the study
      • Participants who are able to be followed up by the participating site
      • Participants planned to receive first line anti-cancer treatment targeting unresectable stage IIIB/IIIC/IV NSCLC in the study site after study initiation
      Exclusion Criteria
      • Participants who have received prior systematic treatment for unresectable Stage IIIB/IIIC/IV NSCLC
      • Participants who have participated in any anti-cancer, regimen-specified clinical study of first-line treatment for unresectable Stage IIIB/IIIC/IV NSCLC

      For the latest version of this information please go to www.forpatients.roche.com

       

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