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

NCT06735781 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 101

Last updated 2024-12-16

No results posted yet for this study

Summary

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

Conditions

  • Non-small Cell Lung Cancer (NSCLC)

Interventions

DRUG

Nivolumab

As prescribed by the treating clinician

Sponsors & Collaborators

Principal Investigators

  • Bristol Myers Squibb · Bristol-Myers Squibb

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-05
Primary Completion
2024-10-01
Completion
2024-10-01
FDA Drug
Yes

Countries

  • France

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06735781 on ClinicalTrials.gov