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    "timestamp_received": "2026-04-24T16:08:32.414021+00:00Z",
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    "name": "Molecular Oncology Almanac",
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  "data": [
    {
      "id": "ind:fda.gavreto:0",
      "indication": "GAVRETO is a kinase inhibitor indicated for treatment of adult patients with metastatic rearranged during transfection (RET) fusion-positive non-small cell lung cancer as detected by an FDA approved test (NSCLC).",
      "initial_approval_date": "2023-08-09",
      "initial_approval_url": "https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/213721s009lbl.pdf",
      "description": "The U.S. Food and Drug Administration granted approval to pralsetinib for the treatment of adult patients with metastatic rearranged during transfection (RET) fusion-positive non-small cell lung cancer, as detected by an FDA approved test (NSCLC).",
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      "raw_cancer_type": "non-small cell lung cancer",
      "raw_therapeutics": "Gavreto (pralsetinib)",
      "icd10": null,
      "regimen_code": null,
      "reimbursement_category": null,
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      "date_accelerated_approval": null,
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        "id": "doc:fda.gavreto",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Gavreto (pralsetinib) [package insert]. FDA.",
        "title": null,
        "aliases": [],
        "description": "Blueprint Medicines Corporation. Gavreto (pralsetinib) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/213721s015lbl.pdf. Revised March 2024. Accessed October 30, 2024.",
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            "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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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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}