{
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    "timestamp_received": "2026-04-23T21:47:51.064029+00:00Z",
    "timestamp_returned": "2026-04-23T21:47:51.067756+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.enhertu:0",
      "indication": "Enhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic HER2-positive breast cancer who have received one or more prior anti-HER2-based regimens.",
      "initial_approval_date": "2022-08-02",
      "initial_approval_url": "https://www.ema.europa.eu/en/documents/variation-report/enhertu-h-c-005124-ii-0014-epar-assessment-report-variation_en.pdf",
      "description": "The European Medicines Agency (EMA) has authorized trastuzumab deruxtecan for the treatment of adult patients with unresectable or metastatic HER2-positive breast cancer who have received one or more prior anti-HER2-based regimes.",
      "raw_biomarkers": null,
      "raw_cancer_type": "Breast cancer",
      "raw_therapeutics": "Enhertu (trastuzumab deruxtecan)",
      "icd10": null,
      "regimen_code": null,
      "reimbursement_category": null,
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      "date_accelerated_approval": null,
      "document": {
        "id": "doc:ema.enhertu",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Enhertu (trastuzumab deruxtecan) [product information]. EMA.",
        "title": null,
        "aliases": [],
        "description": "Daiichi Sankyo Europe GmbH. Enhertu (trastuzumab deruxtecan) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/enhertu-epar-product-information_en.pdf. Revised April 2025. Accessed August 29, 2025.",
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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": "2021-02-08",
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}