Special Drug Use-results Surveillance of Tabrecta Tablets

  • End date
    Mar 31, 2025
  • participants needed
  • sponsor
    Novartis Pharmaceuticals
Updated on 22 September 2023


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)

Condition Non-small Cell Lung Cancer
Treatment Tabrecta tablets
Clinical Study IdentifierNCT04575025
SponsorNovartis Pharmaceuticals
Last Modified on22 September 2023


Yes No Not Sure

Inclusion Criteria

All patients receiving Tabrecta for MET exon 14 skipping mutation-positive unresectable advanced/recurrent NSCLC during a specified post-marketing period

Exclusion Criteria

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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