{
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    "timestamp_received": "2026-04-24T03:20:52.487591+00:00Z",
    "timestamp_returned": "2026-04-24T03:20:52.491490+00:00Z",
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  "service": {
    "github": "https://github.com/vanallenlab/moalmanac-db",
    "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:ema.phesgo:2",
      "indication": "Phesgo is indicated for use in combination with docetaxel in adult patients with HER2-positive metastatic or locally recurrent unresectable breast cancer, who have not received previous anti-HER2 therapy or chemotherapy for their metastatic disease.",
      "initial_approval_date": "2021-01-13",
      "initial_approval_url": "https://www.ema.europa.eu/en/documents/assessment-report/phesgo-epar-public-assessment-report_en.pdf",
      "description": "The European Medicines Agency (EMA) has authorized Phesgo (pertuzumab / trastuzumab) in combination with docetaxel for the treatment of adult patients with HER2-positive metastatic or locally recurrent unresectable breast cancer, who have not received previous anti-HER2 therapy or chemotherapy for their metastatic disease.",
      "raw_biomarkers": null,
      "raw_cancer_type": "Breast cancer",
      "raw_therapeutics": "Phesgo (pertuzumab / trastuzumab) in combination with docetaxel",
      "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:ema.phesgo",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Phesgo (pertuzumab / trastuzumab) [product information]. EMA.",
        "title": null,
        "aliases": [],
        "description": "Roche Registration GmbH. Phesgo (pertuzumab / trastuzumab) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/phesgo-epar-product-information_en.pdf. Revised March 2022. Accessed March 22, 2024.",
        "urls": [
          "https://www.ema.europa.eu/en/medicines/human/EPAR/phesgo",
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        "doi": null,
        "pmid": null,
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              "id": "ema",
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              "description": "Regulatory agency that approves medicines for use in the European Union.",
              "extensions": [
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                  "description": ""
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          {
            "name": "company",
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            "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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          {
            "name": "drug_name_brand",
            "value": "Phesgo",
            "description": "The brand name of the cancer drug, per this document. Only applicable to market authorization documents."
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          {
            "name": "drug_name_generic",
            "value": "pertuzumab / trastuzumab",
            "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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          {
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            "value": "2021-01-13",
            "description": "The publication date for the initial version of this document."
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            "value": null,
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            "value": "2022-03-02",
            "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."
          }
        ]
      }
    }
  ]
}