{
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    "timestamp_received": "2026-04-23T23:25:26.592135+00:00Z",
    "timestamp_returned": "2026-04-23T23:25:26.595979+00:00Z",
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    "github": "https://github.com/vanallenlab/moalmanac-db",
    "name": "Molecular Oncology Almanac",
    "license": "GPL-2.0",
    "release": "draft",
    "url": "https://dev.moalmanac.org",
    "last_updated": "2026-04-09"
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  "data": [
    {
      "id": "ind:ema.revlimid:0",
      "indication": "Revlimid as monotherapy is indicated for the treatment of adult patients with transfusion-dependent anaemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate.",
      "initial_approval_date": "2013-07-19",
      "initial_approval_url": "https://www.ema.europa.eu/en/documents/variation-report/revlimid-h-c-717-ii-0056-epar-assessment-report-variation_en.pdf",
      "description": "The European Medicines Agency (EMA) has authorized lenalidomide for the treatment of adult patients with transfusion-dependent anaemia due to low- or intermdeiate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate.",
      "raw_biomarkers": null,
      "raw_cancer_type": "myelodysplastic syndromes",
      "raw_therapeutics": "Revlimid (lenalidomide)",
      "icd10": null,
      "regimen_code": null,
      "reimbursement_category": null,
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      "date_regular_approval": null,
      "date_accelerated_approval": null,
      "document": {
        "id": "doc:ema.revlimid",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Revlimid (lenalidomide) [product information]. EMA.",
        "title": null,
        "aliases": [],
        "description": "Bristol-Myers Squibb Pharma EEIG. Revlimid (lenalidomide) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/revlimid-epar-product-information_en.pdf. Revised January 2024. Accessed March 28, 2024.",
        "urls": [
          "https://www.ema.europa.eu/en/medicines/human/EPAR/revlimid",
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        ],
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        "pmid": null,
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              "description": "Regulatory agency that approves medicines for use in the European Union.",
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                  "name": "last_updated",
                  "value": "2025-10-01",
                  "description": ""
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                  "value": "https://www.ema.europa.eu/en/medicines",
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            "value": "Bristol-Myers Squibb Pharma EEIG.",
            "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
          },
          {
            "name": "drug_name_brand",
            "value": "Revlimid",
            "description": "The brand name of the cancer drug, per this document. Only applicable to market authorization documents."
          },
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            "name": "drug_name_generic",
            "value": "lenalidomide",
            "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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          {
            "name": "first_publication_date",
            "value": "2009-10-29",
            "description": "The publication date for the initial version of this document."
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            "value": "2024-01-08",
            "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."
          }
        ]
      }
    }
  ]
}