Special Drug Use-results Surveillance of Tabrecta Tablets
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- STATUS
- Recruiting
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- End date
- Mar 31, 2025
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- participants needed
- 100
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- sponsor
- Novartis Pharmaceuticals
Summary
This study is an uncontrolled, primary data collection-based observational study to be conducted as a central registration system, multicenter special drug-use results surveillance. As an all-case study, this study will collect all patients treated with Tabrecta in a specified post-marketing period. The observation period of each patient is up to 1 year (52 weeks)
Details
| Condition | Non-small Cell Lung Cancer |
|---|---|
| Treatment | Tabrecta tablets |
| Clinical Study Identifier | NCT04575025 |
| Sponsor | Novartis Pharmaceuticals |
| Last Modified on | 22 September 2023 |
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