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7LE",{"type":67,"coordinates":2221},[2222,2223],-1.25596,51.75222,{"lat":2223,"lon":2222},{"facility":2226,"status":61,"city":2227,"state":29,"zip":2228,"country":2144,"cosmosGeoPoint":2229,"geoPoint":2233,"contacts":29},"Royal Marsden NHS Foundation Trust","Sutton","SM2 5PT",{"type":67,"coordinates":2230},[2231,2232],-0.2,51.35,{"lat":2232,"lon":2231},{"type":2235,"investigatorFullName":29,"investigatorTitle":29,"investigatorAffiliation":29,"oldNameTitle":29,"oldOrganization":29},"SPONSOR",[2237],{"name":2238,"class":6},"Chugai Pharmaceutical","100577047",false,"NCT06793215","A Study Evaluating the Efficacy and Safety of Divarasib and Pembrolizumab Versus Pembrolizumab and Pemetrexed and Carboplatin or Cisplatin in Participants With Previously Untreated, KRAS G12C-Mutated, Advanced or Metastatic Non-Squamous Non-Small Cell Lung Cancer","A Phase III, Randomized, Open-Label Study Evaluating the Efficacy and Safety of Divarasib and Pembrolizumab Versus Pembrolizumab and Pemetrexed and Carboplatin or Cisplatin in Patients With Previously Untreated, KRAS G12C-Mutated, Advanced or Metastatic Non-Squamous Non-Small Cell Lung Cancer","Krascendo 2","Inclusion Criteria:\n\n* Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1\n* Histologically or cytologically confirmed diagnosis of advanced or metastatic non squamous NSCLC that is not eligible for curative surgery and\u002For definitive chemoradiotherapy\n* Measurable disease, as defined by RECIST v1.1\n* No prior systemic treatment for advanced or metastatic NSCLC\n* Documentation of the presence of a KRAS G12C mutation\n* Documentation of known PD-L1 expression status in tumor tissue\n* Availability of a representative tumor specimen\n* Adequate end-organ function\n* Eligible to receive a platinum-based chemotherapy regimen\n\nExclusion Criteria Related to NSCLC:\n\n* Known concomitant second oncogenic driver with available targeted treatment\n* Symptomatic, untreated, or actively progressing central nervous system (CNS) metastases\n* Spinal cord compression not definitively treated with surgery and\u002For radiation or previously diagnosed and treated spinal cord compression without evidence that disease has been clinically stable for \\>=2 weeks prior to randomization\n* History of leptomeningeal disease\n* Uncontrolled tumor-related pain\n* Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures (once a month or more frequently)\n\nExclusion Criteria Related to Current or Prior Treatments:\n\n* Any anti-cancer systemic therapy, including hormonal therapy, within 21 days prior to randomization, or is expected to require any other form of antineoplastic therapy while in the study\n* Radiation therapy including palliative RT to bone metastases within 2 weeks prior to randomization and RT to the lung \\>30Gy within 6 months prior to randomization\n* Prior treatment with KRAS G12C inhibitors or pan-KRAS\u002FRAS inhibitors\n* Treatment with systemic immunosuppressive or immunostimulatory medications, including CD137 agonists and immune checkpoint inhibitors\n* Current treatment with medications that are well known to prolong the QT interval\n* Treatment with therapeutic oral or IV antibiotics within 2 weeks prior to randomization\n* Prior allogeneic stem cell or solid organ transplantation\n\nExclusion Criteria Related to General Health:\n\n* History of malignancy other than NSCLC within 5 years prior to screening, with the exception of malignancies with a negligible risk of metastasis or death (e.g., 5-year overall survival \\[OS\\] rate \\>90%), such as adequately treated carcinoma in situ of the cervix, non melanoma skin carcinoma, localized prostate cancer, ductal breast carcinoma in situ, or Stage I uterine cancer\n* Individuals with chronic diarrhea, short bowel syndrome or significant upper gastrointestinal surgery including gastric resection, a history of inflammatory bowel disease (e.g., Crohn's disease or ulcerative colitis) or any active bowel inflammation (including diverticulitis), malabsorption syndrome, conditions that would interfere with enteral absorption\n* History of idiopathic pulmonary fibrosis, organizing pneumonia (e.g., bronchiolitis obliterans), drug-induced pneumonitis, or idiopathic pneumonitis, or evidence of active pneumonitis on the screening chest computed tomography scan\n* Significant cardiovascular disease within 3 months prior to screening","ALL","18 Years",{"count":2249,"type":2250},600,"ESTIMATED","INTERVENTIONAL",[2253],"PHASE3","The purpose of this study is to evaluate the efficacy and safety of divarasib and pembrolizumab compared with pembrolizumab and pemetrexed and carboplatin or cisplatin, for the first-line treatment of adult participants with KRAS G12C-mutated, advanced or metastatic non squamous non-small cell lung cancer (NSCLC).",[2256,2257],"Non-Small Cell Lung Cancer","KRAS G12C Lung 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