Comparing the Efficacy and Safety of a New Additional Treatment With Tislelizumab in Non-Small Cell Lung Cancer (NSCLC)
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- STATUS
- Recruiting
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- End date
- Nov 5, 2025
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- participants needed
- 380
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- sponsor
- BeiGene
Summary
The primary objective of this study is to evaluate and compare major pathological response(MPR) rate and event-free survival (EFS) in participants receiving tislelizumab plus platinum-based doublet chemotherapy as the new additional treatment followed by tislelizumab as adjuvant treatment versus participants receiving placebo plus platinum-based doublet chemotherapy as neoadjuvant treatment followed by placebo as adjuvant treatment.
Details
| Condition | Non-Small Cell Lung Cancer, Non-Small Cell Lung Cancer |
|---|---|
| Age | 18-100 years |
| Treatment | Placebos, Carboplatin, tislelizumab, Cisplatin injection, Paclitaxel injection, Pemetrexed Disodium |
| Clinical Study Identifier | NCT04379635 |
| Sponsor | BeiGene |
| Last Modified on | 19 February 2024 |
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