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  • NCT02998528

Active, Not Recruiting

A Neoadjuvant Study of Nivolumab Plus Ipilimumab or Nivolumab Plus Chemotherapy Versus Chemotherapy Alone in Early Stage Non-Small Cell Lung Cancer (NSCLC) - CA209-816

Oppdatert: 12 oktober, 2023   |   ClinicalTrials.gov

Utskriftsvennlig Sammendrag

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  • Phase 3

    Fase

  • Kjønn

  • 18+

    Aldersgruppe

  • Active, Not Recruiting

Behandlingsalternativer

Studiearmer
TILDELT INTERVENSJON
Experimental: Nivolumab plus Ipilimumab
Biological: Ipilimumab, Nivolumab
Experimental: Nivolumab plus platinum doublet chemotherapy
Biological: Nivolumab Drug: Cisplatin, Paclitaxel, Pemetrexed, Carboplatin, Gemcitabine
Active Comparator: Platinum doublet chemotherapy
Drug: Cisplatin, Vinorelbine, Gemcitabine, Paclitaxel, Pemetrexed, Carboplatin, Docetaxel

Nøkkelkriterier for kvalifikasjon

For more information regarding Bristol Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - Early stage IB-IIIA, operable non-small cell lung cancer, confirmed in tissue - Lung function capacity capable of tolerating the proposed lung surgery - Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1 - Available tissue of primary lung tumor Exclusion Criteria: - Presence of locally advanced, inoperable or metastatic disease - Participants with active, known or suspected autoimmune disease - Prior treatment with any drug that targets T cell co-stimulations pathways (such as checkpoint inhibitors) Other protocol defined inclusion/exclusion criteria could apply

Vi anbefaler at du kontakter BMS for å rapportere bivirkninger.
Bivirkninger (uønskede hendelser) og andre rapporterbare hendelser er definert her
For å rapportere bivirkninger (uønskede hendelser) eller reklamere på et legemiddel: Medisinsk informasjon

MLTNO2000046