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Clinical Trial Summary

The study is intended to assess the safety and efficacy of neoadjuvant combination of IPH5201 and durvalumab in addition to standard chemotherapy and adjuvant combination of IPH5201 and durvalumab in untreated patients with resectable, early-stage (stage II to IIIA) non-small cell lung cancer (NSCLC).


Clinical Trial Description

This is an open-label, single-arm multicenter study. Eligible patients will be enrolled and will receive IPH5201 + Durvalumab + standard of care chemotherapy before surgery followed by IPH5201 + Durvalumab post-surgery. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05742607
Study type Interventional
Source Innate Pharma
Contact Innate Pharma
Phone +33484903084
Email clinical.trials@innate-pharma.fr
Status Recruiting
Phase Phase 2
Start date June 23, 2023
Completion date September 2026

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