{
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    "timestamp_received": "2026-04-23T21:47:56.185252+00:00Z",
    "timestamp_returned": "2026-04-23T21:47:56.188928+00:00Z",
    "trace_id": "15b0561d-f0bd-4e05-90b0-53c7cb49a0cb"
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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": "2026-04-09"
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  "data": [
    {
      "id": "ind:ema.lytgobi:0",
      "indication": "Lytgobi monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (FGFR2) fusion or rearrangement that have progressed after at least one prior line of systemic therapy.",
      "initial_approval_date": "2023-07-18",
      "initial_approval_url": "https://www.ema.europa.eu/en/documents/assessment-report/lytgobi-epar-public-assessment-report_en.pdf",
      "description": "The European Medicines Agency (EMA) has given futibatinib conditional market authorization as a monotherapy for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor 2 (FGFR2) fusion or rearrangement that have progressed after at least one line of prior systemic therapy.",
      "raw_biomarkers": null,
      "raw_cancer_type": "Cholangiocarcinoma",
      "raw_therapeutics": "Lytgobi (futibatinib)",
      "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:ema.lytgobi",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Lytgobi (futibatinib) [product information]. EMA.",
        "title": null,
        "aliases": [],
        "description": "Taiho Pharma Netherlands B.V. Lytgobi (futibatinib) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/lytgobi-epar-product-information_en.pdf. Revised October 2023. Accessed March 19, 2024.",
        "urls": [
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        "pmid": null,
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                  "description": ""
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            "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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            "value": "Lytgobi",
            "description": "The brand name of the cancer drug, per this document. Only applicable to market authorization documents."
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            "value": "futibatinib",
            "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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          {
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            "value": "2023-07-18",
            "description": "The publication date for the initial version of this document."
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            "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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        ]
      }
    }
  ]
}