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Patients must sign an informed consent before assessment\n2. Patients with pathologically and\u002For clinically confirmed diagnosis of stage IV non-small (squamous or non-squamous) cell lung cancer (NSCLC) or stage III\u002FIV adenocarcinoma of the pancreas.\n3. Patients with stage IV NSCLC will be receiving or completed or discontinued standard chemotherapy or be chemotherapy-naive by choice.\n4. Patients with stage III\u002FIV pancreatic adenocarcinoma will be receiving standard chemotherapy or no chemotherapy. If patients are receiving chemotherapy, a change in chemotherapy is not expected.\n5. Greater than or equal to 5% unintentional weight loss over the previous 3-6 months, not explained by simple starvation. Simple starvation is considered to be excluded when weight loss is not ameliorated by standard nutritional counseling and oral supplementation over a 2 week period.\n6. Body mass index (BMI) ≤ 30 kg\u002Fm2.\n7. Life expectancy of at least 4 months.\n8. Able to communicate well and comply with the requirements of the study, including by phone and written logs.\n\nKey Exclusion criteria:\n\n1. Patients who have received investigational anti-neoplastic therapy within 3 weeks of screening\n2. Evidence of inadequate organ or brain function, as defined by lab tests and imaging\n3. Patients with severe and\u002For uncontrolled medical conditions that could interfere with the study (e.g. heart conditions, high blood pressure, diabetes, infection) uncontrolled pain or any other non-stable illness\n4. Pregnant or lactating women.\n5. Women capable of becoming pregnant must use highly effective contraception during the study and for 8 weeks after stopping treatment. All female patients must have negative pregnancy test results throughout the study\n6. Patients unwilling or unable to follow instructions.\n\nOther protocol-defined inclusion\u002Fexclusion criteria may apply.",false,"ALL","18 Years",{"count":143,"type":144},57,"ACTUAL","INTERVENTIONAL",[147],"PHASE2","A safety \\& efficacy clinical study of the investigational medicinal product BYM338 for the treatment of unintentional weight loss in patients with cancer of the lung or the pancreas",[150],"Cachexia",[152,153,154,155,156],"Wasting syndrome","emaciation","lung cancer","adenocarcinoma","pancreatic cancer","COMPLETED","2016-02-02",{"date":160,"type":161},"2016-03-02","ESTIMATED",{"date":163,"type":11},"2011-08",{"date":165,"type":144},"2014-04",{"name":29,"class":6},10]