{
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    "message": "Indication id ind:fda.voranigo:0 retrieved successfully",
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    "timestamp_received": "2026-04-24T15:54:50.890354+00:00Z",
    "timestamp_returned": "2026-04-24T15:54:50.894056+00:00Z",
    "trace_id": "c511f735-5a61-48a7-b282-7c676380c705"
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    "name": "Molecular Oncology Almanac",
    "license": "GPL-2.0",
    "release": "draft",
    "url": "https://dev.moalmanac.org",
    "last_updated": "2026-04-09"
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  "data": [
    {
      "id": "ind:fda.voranigo:0",
      "indication": "VORANIGO is an isocitrate dehydrogenase-1 (IDH1) and isocitrate dehydrogenase-2 (IDH2) inhibitor indicated for the treatment of adult and pediatric patients 12 years and older with Grade 2 astrocytoma or oligodendroglioma with a susceptible IDH1 or IDH2 mutation following surgery including biopsy, sub-total resection, or gross total resection.",
      "initial_approval_date": "2024-08-06",
      "initial_approval_url": "https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/218784s000lbl.pdf",
      "description": "The U.S. Food and Drug Administration (FDA) has granted approval to vorasidenib for the treatment of adult and pediatric patients 12 years and older with Grade 2 astrocytoma or oligodendroglioma with a susceptible IDH1 or IDH2 mutation following surgery including biopsy, sub-total resection, or gross total resection.",
      "raw_biomarkers": "IDH1 or IDH2 mutations",
      "raw_cancer_type": "astrocytoma or oligodendroglioma",
      "raw_therapeutics": "vorasidenib",
      "icd10": null,
      "regimen_code": null,
      "reimbursement_category": null,
      "reimbursement_date": null,
      "reimbursement_details": null,
      "date_regular_approval": null,
      "date_accelerated_approval": null,
      "document": {
        "id": "doc:fda.voranigo",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Voranigo (vorasidenib) [package insert]. FDA.",
        "title": null,
        "aliases": [],
        "description": "Servier Pharmaceuticals LLC. Voranigo (vorasidenib) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/218784s000lbl.pdf. Revised August 2024. Accessed October 30, 2024.",
        "urls": [
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          "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=218784"
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        "pmid": null,
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                  "description": ""
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            "description": "The organization that published this document."
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          {
            "name": "company",
            "value": "Servier Pharmaceuticals LLC.",
            "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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          {
            "name": "drug_name_brand",
            "value": "Voranigo",
            "description": "The brand name of the cancer drug, per this document. Only applicable to market authorization documents."
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            "value": "vorasidenib",
            "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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            "value": "2024-08-06",
            "description": "The publication date for the document."
          },
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            "name": "status",
            "value": "Active",
            "description": "Whether this document is Active or Deprecated within moalmanac-db."
          }
        ]
      }
    }
  ]
}