{
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    "message": "Indication id ind:ema:rybrevant:3 retrieved successfully",
    "request_url": "http://api.moalmanac.org/indications?indication_id=ind%3Aema%3Arybrevant%3A3",
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    "timestamp_received": "2026-09-25T06:02:04.007219+00:00Z",
    "timestamp_returned": "2026-09-25T06:02:04.014327+00:00Z",
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    "name": "Molecular Oncology Almanac",
    "license": "GPL-2.0",
    "release": "draft",
    "url": "https://dev.moalmanac.org",
    "last_updated": "2026-08-02"
  },
  "data": [
    {
      "id": "ind:ema:rybrevant:3",
      "type": "Indication",
      "description": "Rybrevant is indicated in combination with lazertinib for the first-line treatment of adult patients with advanced non-small cell lung cancer (NSCLC) with EGFR Exon 19 deletions or Exon 21 L858R substitution mutations.",
      "contributions": [
        {
          "id": "ctrb:ema:2024-12-19:0",
          "type": "Contribution",
          "description": "Indication received approval from the European Commission.",
          "date": "2024-12-19",
          "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": "ctrb:vanallenlab:2024-10-20:0",
          "type": "Contribution",
          "description": "Adding EMA approvals for use to database",
          "date": "2024-10-20",
          "contributor": {
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            "type": "Agent",
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            "name": "Van Allen lab",
            "description": "Van Allen lab, Dana-Farber Cancer Institute"
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          "id": "doc:ema:rybrevant",
          "type": "Document",
          "documentType": "Regulatory approval",
          "name": "Rybrevant (amivantamab) [product information]. EMA.",
          "title": null,
          "aliases": [],
          "description": "Janssen-Cilag International N.V. Rybrevant (amivantamab) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/rybrevant-epar-product-information_en.pdf. Revised July 2025. Accessed September 5, 2025.",
          "urls": [
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          "pmid": null,
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              "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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              "value": "amivantamab",
              "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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              "description": "The publication date for the initial version of this document."
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              "value": null,
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              "value": "2025-07-18",
              "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."
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}