{
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    "timestamp_received": "2026-09-25T06:02:38.179640+00:00Z",
    "timestamp_returned": "2026-09-25T06:02:38.184506+00:00Z",
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    "name": "Molecular Oncology Almanac",
    "license": "GPL-2.0",
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    "url": "https://dev.moalmanac.org",
    "last_updated": "2026-08-02"
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  "data": [
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      "id": "ind:ema:sprycel:0",
      "type": "Indication",
      "description": "SPRYCEL is indicated for the treatment of adult patients with newly diagnosed Philadelphia chromosome positive (Ph+) chronic myelogenous leukaemia (CML) in the chronic phase.",
      "contributions": [
        {
          "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",
            "agentType": "contributor",
            "name": "Van Allen lab",
            "description": "Van Allen lab, Dana-Farber Cancer Institute"
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          "id": "ctrb:ema:2010-12-06:0",
          "type": "Contribution",
          "description": "Indication received approval from the European Commission.",
          "date": "2010-12-06",
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          "id": "doc:ema:sprycel",
          "type": "Document",
          "documentType": "Regulatory approval",
          "name": "Sprycel (dasatinib [anhydrous]) [product information]. EMA.",
          "title": null,
          "aliases": [],
          "description": "Bristol-Myers Squibb Pharma EEIG. Sprycel (dasatinib [anhydrous]) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/sprycel-epar-product-information_en.pdf. Revised June 2022. Accessed March 22, 2024.",
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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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