A Study Describing Real-World Effectiveness of Nivolumab + Chemotherapy in Neoadjuvant NSCLC
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT07141563
- Status
- Completed
Conditions
- Non-small Cell Lung Cancer (NSCLC)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Nivolumab + platinum-based chemotherapy — DRUGAccording to the product label
Study Details
The purpose of this study is to evaluate the real-world effectiveness and safety of neoadjuvant nivolumab combined with chemotherapy in Argentinian patients with resectable non-small cell lung cancer (NSCLC)
Key Dates
- Start date
- May 26, 2025
- Status verified
- Jan 2026
- Primary completion
- Nov 18, 2025
- Completion
- Nov 18, 2025
Study Design
- Enrollment
- 70 participants (actual)
Arms
- Arm: Cohort 1Participants with resectable non-small cell lung cancer (NSCLC) receiving neoadjuvant treatment with nivolumab in combination with platinum-based chemotherapy
Primary Outcome Measure
Rate of pathological complete response (pCR) post-surgery [ Time Frame: Up to 1 year ]
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