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    "timestamp_received": "2026-04-24T03:13:47.328027+00:00Z",
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    "name": "Molecular Oncology Almanac",
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    "url": "https://dev.moalmanac.org",
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  "data": [
    {
      "id": "ind:ema.ziihera:0",
      "indication": "Ziihera as monotherapy is indicated for the treatment of adults with unresectable locally advanced or metastatic HER2-positive (IHC3+) biliary tract cancer (BTC) previously treated with at least one prior line of systemic therapy.",
      "initial_approval_date": "2025-07-03",
      "initial_approval_url": "https://www.ema.europa.eu/en/documents/assessment-report/ziihera-epar-public-assessment-report_en.pdf",
      "description": "The European Medicines Agency (EMA) has authorized zanidatamab for the treatment of adult patients with unresectable locally advanced or metastatic HER2-positive (IHC3+) biliary tract cancer (BTC) previously treated with at least one prior line of systemic therapy.",
      "raw_biomarkers": "HER2-positive (IHC3+)",
      "raw_cancer_type": "biliary tract cancer (BTC)",
      "raw_therapeutics": "Ziihera (zanidatamab)",
      "icd10": null,
      "regimen_code": null,
      "reimbursement_category": null,
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        "id": "doc:ema.ziihera",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Ziihera (zanidatamab) [product information]. EMA.",
        "title": null,
        "aliases": [],
        "description": "Jazz Pharmaceuticals Ireland Limited. Ziihera (zanidatamab) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/ziihera-epar-product-information_en.pdf.pdf. Revised July 2025. Accessed September 8, 2025.",
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            "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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}