{
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    "request_url": "http://api.moalmanac.org/indications?indication_id=ind%3Aema%3Atafinlar%3A4",
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    "timestamp_received": "2026-09-25T06:01:58.737255+00:00Z",
    "timestamp_returned": "2026-09-25T06:01:58.742146+00:00Z",
    "trace_id": "6a3a5782-671c-49d4-b33b-d2df3e71a433"
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    "name": "Molecular Oncology Almanac",
    "license": "GPL-2.0",
    "release": "draft",
    "url": "https://dev.moalmanac.org",
    "last_updated": "2026-08-02"
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  "data": [
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      "id": "ind:ema:tafinlar:4",
      "type": "Indication",
      "description": "Dabrafenib in combination with trametinib is indicated for the adjuvant treatment of adult and adolescents aged 12 years and older with Stage III melanoma with a BRAF V600 mutation, following complete resection.",
      "contributions": [
        {
          "id": "ctrb:ema:2026-04-30:0",
          "type": "Contribution",
          "description": "Indication received approval from the European Commission.",
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            "type": "Agent",
            "agentType": "organization",
            "name": "European Medicines Agency",
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          "id": "ctrb:vanallenlab:2024-10-20:0",
          "type": "Contribution",
          "description": "Adding EMA approvals for use to database",
          "date": "2024-10-20",
          "contributor": {
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            "type": "Agent",
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            "name": "Van Allen lab",
            "description": "Van Allen lab, Dana-Farber Cancer Institute"
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          "id": "doc:ema:tafinlar",
          "type": "Document",
          "documentType": "Regulatory approval",
          "name": "Tafinlar (dabrafenib) [product information]. EMA.",
          "title": null,
          "aliases": [],
          "description": "Novartis Europharm Limited. Tafinlar (dabrafenib) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/tafinlar-epar-product-information_en.pdf. Revised May 2026. Accessed August 2, 2026.",
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              "value": "Novartis Europharm Limited.",
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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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              "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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              "value": "2013-09-18",
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}