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    "name": "Molecular Oncology Almanac",
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  "data": [
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      "indication": "ADCETRIS is indicated for the treatment of adult patients with CD30+ cutaneous T-cell lymphoma (CTCL) after at least 1 prior systemic therapy.",
      "initial_approval_date": "2018-02-01",
      "initial_approval_url": "https://www.ema.europa.eu/en/documents/variation-report/adcetris-h-c-002455-ii-0048-epar-assessment-report-variation_en.pdf",
      "description": "The European Medicines Agency (EMA) has authorized brentuximab vedotin for the treatment of adult patients with CD30+ cutaneous T-cell lymphoma (CTCL) after at least 1 prior systemic therapy.",
      "raw_biomarkers": null,
      "raw_cancer_type": "Cutaneous T-cell lymphoma (CTCL)",
      "raw_therapeutics": "Adcetris (brentuximab vedotin)",
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        "name": "Adcetris (brentuximab vedotin) [product information]. EMA.",
        "title": null,
        "aliases": [],
        "description": "Takeda Pharma A/S. Adcetris (brentuximab vedotin) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/adcetris-epar-product-information_en.pdf. Revised December 2023. Accessed March 11, 2024.",
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