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  • NCT06169956

Recruiting

An Observational Study to Evaluate Neoadjuvant Nivolumab (OPDIVO®) in Combination With Platinum-Based Chemotherapy in Non-Metastatic Non-Small Cell Lung Cancer Participants in Germany - CA209-1210

Opdateret: 17 april, 2024   |   ClinicalTrials.gov

Udskriftsvenligt sammendrag

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VÆLG SPROG

Forsøgsdetaljer

  • Køn

  • 18+

    Aldersinterval

  • 1

    Beliggenhed(er)

  • Recruiting

Behandlingsmuligheder

Forsøgsgrene
TILDELT INTERVENTION
Participants receiving neoadjuvant nivolumab in combination with platinum-based chemotherapy
Drug: Neoadjuvant nivolumab in combination with platinum-based chemotherapy

Primære egnethedskriterier

Inclusion Criteria: - Aged 18 years or older - Diagnosis of non-metastatic non-small cell lung cancer with tumor Programmed death-ligand 1 (PD-L1) expression level of 1% or more (tumor proportion score (TPS); according to label approved in the European Union) - Decision to initiate a neoadjuvant treatment with nivolumab plus platinum-based chemotherapy for treatment of non-small cell lung cancer according to current Summary of product characteristics and independent of the study - Willing to complete patient-reported outcome questionnaires and sufficient understanding of the German language - Signed written informed consent - Other criteria according to current Summary of product characteristics Exclusion Criteria: - Current primary diagnosis of cancer other than non-small cell lung cancer that requires systemic or other treatment - Other contraindications according to current Summary of product characteristics

Hvis du vil rapportere en bivirkning, kan du indberette direkte til Lægemiddelstyrelsen via hjemmesiden www.meldenbivirkning.dk
Vi anbefaler at du også kontakter BMS for at rapportere bivirkninger.
Bivirkninger og andre rapporterbare begivenheder er defineret her
Rapporter bivirkninger eller klager over produktkvalitet: Medicinsk information

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