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Content last updated November 15, 2011.
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|Company||Genentech Inc (Roche Holding AG)|
|Highest Dev Status||Launched|
|FDA Approved||Glioblastoma Multiforme Of Brain, Recurrent, Progressive Disease Following Prior Therapy (Adult), Metastatic Breast Cancer, Her2-Negative, As First-Line Therapy In Combination With Paclitaxel (Adult), Metastatic Colorectal Cancer, First- Or Second-Line Therapy, In Combination With 5-Fluorouracil-Based Chemotherapy (Adult), Metastatic Renal Cell Carcinoma, In Combination With Interferon Alfa (Adult), Nonsquamous Non-Small Cell Lung Cancer, Recurrent Or Metastatic, Unresectable, Locally Advanced, First-Line Treatment In Combination With Paclitaxel And Carboplatin (Adult)|
|Therapy Areas||Neuroendocrine tumor; Age related macular degeneration; Mesothelioma; Small-cell lung cancer; Non-small-cell lung cancer; Stomach tumor; Myelodysplastic syndrome; Biliary cancer; Endometroid carcinoma; Renal cell carcinoma; Hepatocellular carcinoma; Multiple myeloma; Sarcoma; Melanoma; Fallopian tube cancer; Glioblastoma; Pancreas tumor; Carcinoid tumor; Peritoneal tumor; B-cell lymphoma; Non-Hodgkin lymphoma; Gastrointestinal stromal tumor; Hormone refractory prostate cancer; Breast tumor; Genitourinary tract tumor; Head and neck tumor; Colon tumor; Ovary tumor; Colorectal tumor|
|Actions||VEGF ligand inhibitor; Anticancer monoclonal antibody; Angiogenesis inhibitor|
|Technologies||Monoclonal antibody humanized; Intravenous formulation; Infusion; Biological therapeutic|
|Reason for update||Minor editorial amendment|