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    "name": "Molecular Oncology Almanac",
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  "data": [
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      "id": "ind:ema.cyramza:0",
      "indication": "Cyramza in combination with erlotinib is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer with activating epidermal growth factor receptor (EGFR) mutations.",
      "initial_approval_date": "2020-02-20",
      "initial_approval_url": "https://www.ema.europa.eu/en/documents/variation-report/cyramza-h-c-2829-ii-0033-epar-assessment-report-variation_en.pdf",
      "description": "The European Medicines Agency (EMA) has authorized ramucirumab in combination with erlotinib as a first-line treatment for adult patients with metastatic non-small cell lung cancer with activating EGFR variants.",
      "raw_biomarkers": null,
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        "id": "doc:ema.cyramza",
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        "name": "Cyramza (ramucirumab) [product information]. EMA.",
        "title": null,
        "aliases": [],
        "description": "Eli Lilly Nederland B.V. Cyramza (ramucirumab) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/cyramza-epar-product-information_en.pdf. Revised December 2022. Accessed March 7, 2024.",
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