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2SJ",{"type":82,"coordinates":2310},[2311,2312],-1.4659,53.38297,{"lat":2312,"lon":2311},{"facility":2315,"status":75,"city":2316,"state":11,"zip":2317,"country":2193,"countryCode":2194,"cosmosGeoPoint":2318,"geoPoint":2322,"contacts":11},"Southampton General Hospital","Southampton","SO16 6YD",{"type":82,"coordinates":2319},[2320,2321],-1.40428,50.90395,{"lat":2321,"lon":2320},{"facility":2324,"status":75,"city":2325,"state":11,"zip":2326,"country":2193,"countryCode":2194,"cosmosGeoPoint":2327,"geoPoint":2331,"contacts":11},"Musgrove Park Hospital-Taunton & Somerset NHS Foundation Trust","Taunton","TA1 5DA",{"type":82,"coordinates":2328},[2329,2330],-3.10293,51.01494,{"lat":2330,"lon":2329},{"facility":2333,"status":75,"city":2334,"state":11,"zip":2335,"country":2193,"countryCode":2194,"cosmosGeoPoint":2336,"geoPoint":2340,"contacts":11},"New Cross Hospital","Wolverhampton","WV10 0QP",{"type":82,"coordinates":2337},[2338,2339],-2.12296,52.58547,{"lat":2339,"lon":2338},{"type":2342,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR",[2344],{"name":2345,"class":6},"Bristol-Myers Squibb","100570828","phase-2-safety-efficacy-and-pharmacokinetics-of-bnt327-in-combination-with-chemotherapy-and-other-investigational-agents-for-lung-cancer-100570828",false,"NCT06712316","Safety, Efficacy, and Pharmacokinetics of BNT327 in Combination With Chemotherapy and Other Investigational Agents for Lung Cancer","A Phase II\u002FIII, Multisite, Randomized Master Protocol for a Global Trial of BNT327 in Combination With Chemotherapy and Other Investigational Agents in First-line Non-small Cell Lung Cancer","Key Inclusion Criteria:\n\n* Have systemic treatment naive, histologically or cytologically confirmed diagnosis of Stage IIIB or IIIC (who are not amenable to curative surgery or radiotherapy) or Stage IV NSCLC per the Union Internationale contre le Cancer\u002FAmerican Joint Committee on Cancer staging system, 9th edition.\n* Have at least one measurable lesion as the targeted lesion based on RECIST v1.1. Lesions treated after prior local treatment (radiotherapy, ablation, interventional procedures, etc.) are generally not considered as target lesions. If the lesion with prior local treatment is the only targeted lesion, evidence-based radiology must be provided to demonstrate disease progression (the single bone metastasis or the single central nervous system metastasis should not be considered as a measurable lesion).\n* Eastern Cooperative Oncology Group Performance Status of 0 or 1.\n* Adequate organ function.\n\nKey Exclusion Criteria:\n\n* Have histologically or cytologically confirmed NSCLC with small-cell lung cancer histologic or neuroendocrine component.\n* Have received any of the following therapies or drugs within the noted time intervals prior to study treatment:\n\n  * Previous chemotherapy (platinum-based) or PD(L)-1 for treating NSCLC in either neo-adjuvant\u002Fadjuvant or locally advanced\u002Fmetastatic setting.\n  * Participants who received prior treatment with anti-VEGF monoclonal antibody, or PD(L)-1\u002FVEGF bispecific antibody\n  * Have received systemic corticosteroids (at a dosage greater than 10 mg\u002Fday of prednisone or an equivalent dose of other corticosteroids) within 7 days prior to the initiation of study treatment. Note: local, intranasal, intraocular, intra-articular or inhaled corticosteroids, short-term use (\\\u003C=7 days) of corticosteroids for prophylaxis (e.g., prevention of contrast agent allergy) or treatment of non-autoimmune conditions (e.g., delayed hypersensitivity reactions caused by exposure to allergens) are allowed.\n* Have uncontrolled hypertension or poorly controlled diabetic conditions prior to study treatment.\n* Have a serious or non-healing wound, or (incompletely healed) bone fracture. This includes history (within 6 months prior to study entry) or risk of abdominal fistula, tracheoesophageal fistula, gastrointestinal perforation, or intra-abdominal abscess or esophageal and gastric varices. In addition, the participant must have undergone correction (or spontaneous healing) of the perforation\u002Ffistula and\u002For the underlying process causing fistula\u002Fperforation.\n* Participants with significant risk of hemorrhage (per investigator clinical judgment).\n* Have superior vena cava syndrome or symptoms of spinal cord compression.\n\nNOTE: Other protocol defined Inclusion\u002FExclusion criteria may apply.","ALL","18 Years",{"count":2356,"type":2357},1260,"ESTIMATED","INTERVENTIONAL",[2360,2361],"PHASE2","PHASE3","This is a Phase 2\u002F3, multisite, randomized, open-label study in participants with first-line non-small cell lung cancer (NSCLC).\n\nThis study includes two substudies (substudy A and substudy B) that will recruit participants according to histological subtypes due to differences in chemotherapy choice for standard-of-care and type of NSCLC.",[2364],"Non-small Cell Lung Cancer",[2366,2367,2368,2369,2370,2371,2372,2373],"First-line treatment","Combination with chemotherapy","Combination with other investigational agents","Bispecific antibody","Programmed death-ligand 1 (PD-L1)","Vascular endothelial growth factor (VEGF) A","Immunotherapy","Programmed Death-1 monoclonal antibodies","2026-06-30",{"date":2376,"type":2377},"2026-07-01","ACTUAL",{"date":2379,"type":2377},"2025-01-07",{"date":2381,"type":2357},"2030-03",{"name":5,"class":6},261]