{
  "meta": {
    "data_length": 1,
    "message": "Indication id ind:ema:voranigo:0 retrieved successfully",
    "request_url": "http://api.moalmanac.org/indications?indication_id=ind%3Aema%3Avoranigo%3A0",
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    "timestamp_received": "2026-09-25T06:04:21.002184+00:00Z",
    "timestamp_returned": "2026-09-25T06:04:21.003701+00:00Z",
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    "name": "Molecular Oncology Almanac",
    "license": "GPL-2.0",
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    "url": "https://dev.moalmanac.org",
    "last_updated": "2026-08-02"
  },
  "data": [
    {
      "id": "ind:ema:voranigo:0",
      "type": "Indication",
      "description": "Voranigo as monotherapy is indicated for the treatment of predominantly non-enhancing Grade 2 astrocytoma or oligodendroglioma with an IDH1 R132 or IDH2 R172 mutation in adult and adolescent patients aged 12 years and older and weighing at least 40 kg who only had surgical intervention and are not in immediate need of radiotherapy or chemotherapy.",
      "contributions": [
        {
          "id": "ctrb:vanallenlab:2025-10-02:2",
          "type": "Contribution",
          "description": "On 2025-09-26 the EMA granted initial market authorization to Voranigo (vorasidenib) for the treatment of patients with astrocytoma or oligodendroglioma with an IDH1 R132 or IDH2 R172 mutation.",
          "date": "2025-10-02",
          "contributor": {
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            "type": "Agent",
            "agentType": "contributor",
            "name": "Van Allen lab",
            "description": "Van Allen lab, Dana-Farber Cancer Institute"
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        {
          "id": "ctrb:ema:2025-09-17:0",
          "type": "Contribution",
          "description": "Indication received approval from the European Commission.",
          "date": "2025-09-17",
          "contributor": {
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            "type": "Agent",
            "agentType": "organization",
            "name": "European Medicines Agency",
            "description": "Regulatory agency that approves medicines for use in the European Union."
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          "id": "doc:ema:voranigo",
          "type": "Document",
          "documentType": "Regulatory approval",
          "name": "Voranigo (vorasidenib) [product information]. EMA.",
          "title": null,
          "aliases": [],
          "description": "Les Laboratoires Servier. Voranigo (vorasidenib) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/voranigo-epar-product-information_en.pdf. Revised September 2025. Accessed October 2, 2025.",
          "urls": [
            "https://www.ema.europa.eu/en/documents/product-information/voranigo-epar-product-information_en.pdf",
            "https://www.ema.europa.eu/en/medicines/human/EPAR/voranigo"
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          "pmid": null,
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              "value": "Les Laboratoires Servier",
              "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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              "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": "2025-09-26",
              "description": "The publication date for the initial version of this document."
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              "value": null,
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              "value": "2025-09-26",
              "description": "The publication date for the document."
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              "description": "Whether this document is Active or Deprecated within moalmanac-db."
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      "extensions": [
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}