{
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    "timestamp_received": "2026-09-25T00:12:57.631226+00:00Z",
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    "name": "Molecular Oncology Almanac",
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    "url": "https://dev.moalmanac.org",
    "last_updated": "2026-08-02"
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  "data": [
    {
      "id": "ind:fda:verzenio:2",
      "type": "Indication",
      "description": "Verzenio is a kinase inhibitor indicated in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer with disease progression following endocrine therapy.",
      "contributions": [
        {
          "id": "ctrb:vanallenlab:2024-10-30:0",
          "type": "Contribution",
          "description": "Initial access of FDA approvals",
          "date": "2024-10-30",
          "contributor": {
            "id": "agent:user:vanallenlab",
            "type": "Agent",
            "agentType": "contributor",
            "name": "Van Allen lab",
            "description": "Van Allen lab, Dana-Farber Cancer Institute"
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        {
          "id": "ctrb:fda:2017-09-28:0",
          "type": "Contribution",
          "description": "Indication received traditional approval.",
          "date": "2017-09-28",
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            "type": "Agent",
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          "id": "doc:fda:verzenio",
          "type": "Document",
          "documentType": "Regulatory approval",
          "name": "Verzenio (abemaciclib) [package insert]. FDA.",
          "title": null,
          "aliases": [],
          "description": "Eli and Lily Company. Verzenio (abemaciclib) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/208716s010s011lbl.pdf. Revised March 2023. Accessed October 30, 2024.",
          "urls": [
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              "name": "company",
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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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              "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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