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    "timestamp_received": "2026-04-06T14:46:53.464112+00:00Z",
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    "name": "Molecular Oncology Almanac",
    "license": "GPL-2.0",
    "release": "draft",
    "url": "https://dev.moalmanac.org",
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  "data": [
    {
      "id": "ind:fda.retevmo:1",
      "indication": "RETEVMO is a kinase inhibitor indicated for the treatment of adult and pediatric patients 2 years of age and older with advanced or metastatic medullary thyroid cancer (MTC) with a RET mutation, as detected by an FDA-approved test, who require systemic therapy.",
      "initial_approval_date": "2024-05-29",
      "initial_approval_url": "https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/213246s012lbl.pdf",
      "description": "The U.S. Food and Drug Administration granted approval to selpercatinib for the treatment of adult and pediatric patients 2 years of age and older with advanced or metastatic medullary thyroid cancer (MTC) with a RET mutation, as detected by an FDA-approved test, who require systemic therapy.",
      "raw_biomarkers": "RET mutation",
      "raw_cancer_type": "advanced or metastatic medullary thyroid cancer",
      "raw_therapeutics": "Retevmo (selpercatinib)",
      "icd10": null,
      "regimen_code": null,
      "reimbursement_category": null,
      "reimbursement_date": null,
      "reimbursement_details": null,
      "date_regular_approval": "2024-09-27",
      "date_accelerated_approval": "2024-05-29",
      "document": {
        "id": "doc:fda.retevmo",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Retevmo (selpercatinib) [package insert]. FDA.",
        "title": null,
        "aliases": [],
        "description": "Eli Lilly and Company. Retevmo (selpercatinib) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/213246s011s013lbl.pdf. Revised September 2024. Accessed October 30, 2024.",
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            "value": "Eli Lilly and Company.",
            "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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            "value": "Retevmo",
            "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": "2020-05-08",
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}