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2ES",{"type":68,"coordinates":2364},[2365,2366],-0.12574,51.50853,{"lat":2366,"lon":2365},{"facility":2369,"status":61,"city":2361,"state":29,"zip":2370,"country":2316,"countryCode":2317,"cosmosGeoPoint":2371,"geoPoint":2373,"contacts":29},"Royal Marsden Hospital - Fulham","SW3 6JJ",{"type":68,"coordinates":2372},[2365,2366],{"lat":2366,"lon":2365},{"facility":2375,"status":61,"city":2361,"state":29,"zip":2376,"country":2316,"countryCode":2317,"cosmosGeoPoint":2377,"geoPoint":2379,"contacts":29},"Sarah Cannon Research Institute","W1G 6AD",{"type":68,"coordinates":2378},[2365,2366],{"lat":2366,"lon":2365},{"facility":2381,"status":61,"city":2382,"state":29,"zip":2383,"country":2316,"countryCode":2317,"cosmosGeoPoint":2384,"geoPoint":2388,"contacts":29},"Maidstone and Tunbridge Wells NHS Trust","Maidstone","ME16 9QQ",{"type":68,"coordinates":2385},[2386,2387],0.51667,51.26667,{"lat":2387,"lon":2386},{"facility":2390,"status":61,"city":2391,"state":29,"zip":2392,"country":2316,"countryCode":2317,"cosmosGeoPoint":2393,"geoPoint":2397,"contacts":29},"Oxford University Hospitals NHS Trust - Churchill Hospital","Oxford","OX3 7LE",{"type":68,"coordinates":2394},[2395,2396],-1.25596,51.75222,{"lat":2396,"lon":2395},{"facility":2399,"status":61,"city":2400,"state":29,"zip":2401,"country":2316,"countryCode":2317,"cosmosGeoPoint":2402,"geoPoint":2406,"contacts":29},"Royal Marsden NHS Foundation Trust","Sutton","SM2 5PT",{"type":68,"coordinates":2403},[2404,2405],-0.2,51.35,{"lat":2405,"lon":2404},{"type":2408,"investigatorFullName":29,"investigatorTitle":29,"investigatorAffiliation":29,"oldNameTitle":29,"oldOrganization":29},"SPONSOR",[2410],{"name":2411,"class":6},"Chugai Pharmaceutical","100577047","phase-3-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-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":2423,"type":2424},600,"ESTIMATED","INTERVENTIONAL",[2427],"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).",[2430,2431],"Non-Small Cell Lung Cancer","KRAS G12C Lung Cancer",[2433,2434,2435,2436,26,2437,2438,2439,2440,2441],"Advanced Non-Small Cell Lung Cancer","KRAS G12 Lung Cancer","Advanced Lung Cancer","Metastatic lung cancer","KRAS G12C Inhibitor","KRAS G12C Positive","KRAS Mutation","KRAS G12C Mutation","Lung Cancer Mutation","2026-08-04",{"date":2444,"type":2445},"2026-08-06","ACTUAL",{"date":2447,"type":2445},"2025-10-24",{"date":2449,"type":2424},"2030-10-31",{"name":5,"class":6},268]