Clinical Outcomes of Patients With Resectable Non-Small Cell Lung Cancer Receiving Neoadjuvant Nivolumab Plus Chemotherapy in France

Last updated: December 11, 2024
Sponsor: Bristol-Myers Squibb
Overall Status: Completed

Phase

N/A

Condition

N/A

Treatment

Nivolumab

Clinical Study ID

NCT06735781
CA209-1512
  • Ages > 18
  • All Genders

Study Summary

The purpose of this study is to evaluate real-world effectiveness of neoadjuvant nivolumab plus chemotherapy in France.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Having a diagnosis of resectable non-small cell lung cancer (NSCLC)

  • Being 18 years or above at the time of their NSCLC diagnosis

  • Having initiated a neoadjuvant treatment with nivolumab and chemotherapy outside aclinical trial

  • Being indexed in the site database

  • Being followed at the site for at least 5 months, except for patients with a recordof death

Exclusion

Exclusion Criteria:

• Having any primary tumor other than NSCLC on or before the date of NSCLC diagnosis that required a treatment ending less than 12-months before the nivolumab plus chemotherapy neoadjuvant treatment

Study Design

Total Participants: 101
Treatment Group(s): 1
Primary Treatment: Nivolumab
Phase:
Study Start date:
September 05, 2024
Estimated Completion Date:
October 01, 2024

Connect with a study center

  • Centre François Baclesse

    Caen,
    France

    Site Not Available

  • Centre Léon Bérard

    Lyon,
    France

    Site Not Available

  • Hospices Civils de Lyon

    Lyon,
    France

    Site Not Available

  • Hôpital Robert Schuman

    Metz,
    France

    Site Not Available

  • Institut du Cancer de Montpellier

    Montpellier,
    France

    Site Not Available

  • Institute Curie

    Paris,
    France

    Site Not Available

  • Hôpital d'Instruction des Armées Saint Anne

    Toulon,
    France

    Site Not Available

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