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      "id": "ind:ema:erbitux:0",
      "type": "Indication",
      "description": "Erbitux is indicated for the treatment of patients with epidermal growth factor receptor (EGFR)-expressing, RAS wild-type metastatic colorectal cancer as a single agent in patients who have failed oxaliplatin- and irinotecan-based therapy and who are intolerant to irinotecan.",
      "contributions": [
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          "type": "Contribution",
          "description": "Adding EMA approvals for use to database",
          "date": "2024-10-20",
          "contributor": {
            "id": "agent:user:vanallenlab",
            "type": "Agent",
            "agentType": "contributor",
            "name": "Van Allen lab",
            "description": "Van Allen lab, Dana-Farber Cancer Institute"
          }
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        {
          "id": "ctrb:ema:2008-07-17:0",
          "type": "Contribution",
          "description": "Indication received approval from the European Commission.",
          "date": "2008-07-17",
          "contributor": {
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            "type": "Agent",
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            "name": "European Medicines Agency",
            "description": "Regulatory agency that approves medicines for use in the European Union."
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          "id": "doc:ema:erbitux",
          "type": "Document",
          "documentType": "Regulatory approval",
          "name": "Erbitux (cetuximab) [product information]. EMA.",
          "title": null,
          "aliases": [],
          "description": "Merck Europe B.V. Erbitux (cetuximab) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/erbitux-epar-product-information_en.pdf. Revised July 2026. Accessed August 2, 2026.",
          "urls": [
            "https://www.ema.europa.eu/en/documents/product-information/erbitux-epar-product-information_en.pdf",
            "https://www.ema.europa.eu/en/medicines/human/EPAR/erbitux"
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              "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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              "description": "The brand name of the cancer drug, per this document. Only applicable to market authorization documents."
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              "value": "cetuximab",
              "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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              "description": "The publication date for the document."
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          "description": "The description text for all Statements derived from this Indication."
        }
      ]
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  ]
}