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    "timestamp_received": "2026-04-23T21:47:55.685469+00:00Z",
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    "name": "Molecular Oncology Almanac",
    "license": "GPL-2.0",
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    "url": "https://dev.moalmanac.org",
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  "data": [
    {
      "id": "ind:ema.venclyxto:0",
      "indication": "Venclyxto monotherapy is indicated for the treatment of CLL in the presence of 17p deletion or TP53 mutation in adult patients who are unsuitable for or have failed a B-cell receptor pathway inhibitor.",
      "initial_approval_date": "2016-12-21",
      "initial_approval_url": "https://www.ema.europa.eu/en/documents/assessment-report/venclyxto-epar-public-assessment-report_en.pdf",
      "description": "The European Medicines Agency (EMA) has authorized venetoclax as a monotherapy for the treatment of patients with chronic lymphocytic leukemia (CLL) in the presence of 17p deletion or TP53 mutation in adult patients who are unsuitable for or have failed a B-cell receptor pathway inhibitor.",
      "raw_biomarkers": null,
      "raw_cancer_type": "Chronic lymphocytic leukemia (CLL)",
      "raw_therapeutics": "Venclyxto (venetoclax)",
      "icd10": null,
      "regimen_code": null,
      "reimbursement_category": null,
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        "id": "doc:ema.venclyxto",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Venclyxto (venetoclax) [product information]. EMA.",
        "title": null,
        "aliases": [],
        "description": "AbbVie Deutschland GmbH Co. KG. Venclyxto (venetoclax) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/venclyxto-epar-product-information_en.pdf. Revised October 2022. Accessed March 25, 2024.",
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}