{
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    "message": "Indication id ind:hc.keytruda:6 retrieved successfully",
    "request_url": "http://api.moalmanac.org/indications?indication_id=ind%3Ahc.keytruda%3A6",
    "status": "success",
    "status_code": 200,
    "timestamp_elapsed": 0.003565,
    "timestamp_received": "2026-04-06T14:46:25.744367+00:00Z",
    "timestamp_returned": "2026-04-06T14:46:25.747932+00:00Z",
    "trace_id": "58ae9c6e-03f6-45b8-9b2c-2b9a9cec48f0"
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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": "2026-03-05"
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  "data": [
    {
      "id": "ind:hc.keytruda:6",
      "indication": "KEYTRUDA (pembrolizumab), in combination with lenvatinib, is indicated for the treatment of adult patients with advanced endometrial carcinoma that is not microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR), who have disease progression following prior platinum-based systemic therapy, and are not candidates for curative surgery or radiation.",
      "initial_approval_date": null,
      "initial_approval_url": null,
      "description": "Health Canada approved pembrolizumab in combination with lenvatinib for the treatment of adult patients with advanced endometrial carcinoma that is not microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR), who have disease progression following prior platinum-based systemic therapy, and are not candidates for curative surgery or radiation.",
      "raw_biomarkers": "not MSI-H or dMMR",
      "raw_cancer_type": "advanced endometrial carcinoma",
      "raw_therapeutics": "Keytruda (pembrolizumab), lenvatinib",
      "icd10": null,
      "regimen_code": null,
      "reimbursement_category": null,
      "reimbursement_date": null,
      "reimbursement_details": null,
      "date_regular_approval": null,
      "date_accelerated_approval": null,
      "document": {
        "id": "doc:hc.keytruda",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Keytruda (pembrolizumab) [product monograph]. HC.",
        "title": null,
        "aliases": [],
        "description": "Merck Canada Inc. Keytruda (pembrolizumab) [product monograph]. Health Canada website. https://pdf.hres.ca/dpd_pm/00080285.PDF. Published April 2025. Accessed June 2025.",
        "urls": [
          "https://health-products.canada.ca/dpd-bdpp/info?lang=eng&code=94388",
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        "pmid": null,
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                  "description": ""
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            },
            "description": "The organization that published this document."
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            "value": "Merck Canada Inc.",
            "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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            "value": "Keytruda",
            "description": "The brand name of the cancer drug, per this document. Only applicable to market authorization documents."
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            "value": "pembrolizumab",
            "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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            "value": "2025-04-11",
            "description": "The publication date for the initial version of this document."
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            "value": null,
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            "value": "2025-04-11",
            "description": "The publication date for the document."
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          {
            "name": "status",
            "value": "Active",
            "description": "Whether this document is Active or Deprecated within moalmanac-db."
          }
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      }
    }
  ]
}