{
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    "data_length": 1,
    "message": "Indication id ind:ema:herceptin:1 retrieved successfully",
    "request_url": "http://api.moalmanac.org/indications?indication_id=ind%3Aema%3Aherceptin%3A1",
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    "timestamp_received": "2026-09-25T06:04:19.973207+00:00Z",
    "timestamp_returned": "2026-09-25T06:04:19.974781+00:00Z",
    "trace_id": "870341f8-edda-4842-9050-380065d453f4"
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  "service": {
    "github": "https://github.com/vanallenlab/moalmanac-db",
    "name": "Molecular Oncology Almanac",
    "license": "GPL-2.0",
    "release": "draft",
    "url": "https://dev.moalmanac.org",
    "last_updated": "2026-08-02"
  },
  "data": [
    {
      "id": "ind:ema:herceptin:1",
      "type": "Indication",
      "description": "Herceptin is indicated for the treatment of adult patients with HER2 positive metastatic breast cancer (MBC) in combination with paclitaxel for the treatment of those patients who have not received chemotherapy for their metastatic disease and for whom an anthracycline is not suitable.",
      "contributions": [
        {
          "id": "ctrb:vanallenlab:2024-10-20:0",
          "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"
          }
        },
        {
          "id": "ctrb:ema:2000-08-28:0",
          "type": "Contribution",
          "description": "Indication received approval from the European Commission.",
          "date": "2000-08-28",
          "contributor": {
            "id": "agent:org:ema",
            "type": "Agent",
            "agentType": "organization",
            "name": "European Medicines Agency",
            "description": "Regulatory agency that approves medicines for use in the European Union."
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          "id": "doc:ema:herceptin",
          "type": "Document",
          "documentType": "Regulatory approval",
          "name": "Herceptin (trastuzumab) [product information]. EMA.",
          "title": null,
          "aliases": [],
          "description": "Roche Registration GmbH. Herceptin (trastuzumab) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/herceptin-epar-product-information_en.pdf. Revised March 2023. Accessed March 12, 2024.",
          "urls": [
            "https://www.ema.europa.eu/en/documents/product-information/herceptin-epar-product-information_en.pdf",
            "https://www.ema.europa.eu/en/medicines/human/EPAR/herceptin"
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          "pmid": null,
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              "name": "company",
              "value": "Roche Registration GmbH.",
              "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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              "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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              "value": "2010-03-01",
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              "value": "2023-03-17",
              "description": "The publication date for the document."
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              "description": "Whether this document is Active or Deprecated within moalmanac-db."
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}