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      "id": "ind:ema:keytruda:12",
      "type": "Indication",
      "description": "KEYTRUDA, in combination with chemotherapy with or without bevacizumab, is indicated for the treatment of persistent, recurrent, or metastatic cervical cancer in adults whose tumours express PD-L1 with a CPS >= 1.",
      "contributions": [
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          "type": "Contribution",
          "description": "Adding EMA approvals for use to database",
          "date": "2024-10-20",
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            "name": "Van Allen lab",
            "description": "Van Allen lab, Dana-Farber Cancer Institute"
          }
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          "id": "ctrb:ema:2022-04-25:0",
          "type": "Contribution",
          "description": "Indication received approval from the European Commission.",
          "date": "2022-04-25",
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          "id": "doc:ema:keytruda",
          "type": "Document",
          "documentType": "Regulatory approval",
          "name": "Keytruda (pembrolizumab) [product information]. EMA.",
          "title": null,
          "aliases": [],
          "description": "Merck Sharp & Dohme B.V. Keytruda (pembrolizumab) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/keytruda-epar-product-information_en.pdf. Revised January 2024. Accessed March 10, 2024.",
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          "description": "The description text for all Statements derived from this Indication."
        }
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}