{
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    "timestamp_received": "2026-11-09T16:14:09.180033Z",
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    "name": "Molecular Oncology Almanac",
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      "id": "ind:hse:00588:h",
      "type": "Indication",
      "description": "As monotherapy or in combination with endocrine therapy for the adjuvant treatment of adult patients with germline BRCA1/2-mutations who have HER2-negative high risk early breast cancer previously treated with neoadjuvant or adjuvant chemotherapy. Lynparza's product information fromcites the OlympiA trial, where olaparib was compared against placebo for the treatment of patients with germline BRCA1/2 mutated and HER2-negative high risk early breast cancer.",
      "contributions": [
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          "id": "ctrb:hse:2025-05-01:0",
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          "date": "2025-05-01",
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          "date": "2024-01-16",
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            "name": "Van Allen lab",
            "description": "Van Allen lab, Dana-Farber Cancer Institute"
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          "id": "doc:hse:00588",
          "type": "Document",
          "documentType": "Regulatory approval",
          "name": "Olaparib (Tablet) Monotherapy. NCCP National SACT Regimen. HSE.",
          "title": null,
          "aliases": [],
          "description": "Olaparib (Tablet) Monotherapy, 2025, version number 5b, NCCP National SACT Regimen, NCCP, viewed 26/03/2026, https://healthservice.hse.ie/documents/6397/588_V5b_olaparib_tablet_monotherapy.pdf",
          "urls": [
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              "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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          "description": "The description text for all Statements derived from this Indication."
        },
        {
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          "value": "CDS",
          "description": "Current scheme used to reimburse indication."
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        {
          "name": "reimbursement_comment",
          "value": null,
          "description": "More details about the current reimbursement scheme(s)."
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}