{
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    "message": "Indication id ind:ema.elahere:0 retrieved successfully",
    "request_url": "http://api.moalmanac.org/indications?indication_id=ind%3Aema.elahere%3A0",
    "status": "success",
    "status_code": 200,
    "timestamp_elapsed": 0.004005,
    "timestamp_received": "2026-04-24T03:10:32.523855+00:00Z",
    "timestamp_returned": "2026-04-24T03:10:32.527860+00:00Z",
    "trace_id": "9530772f-33ba-40a5-8482-f39375f92d28"
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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"
  },
  "data": [
    {
      "id": "ind:ema.elahere:0",
      "indication": "ELAHERE as monotherapy is indicated for the treatment of adult patients with folate receptor-alpha (FDalpha) positive, platinum-resistant high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who have received one to three prior systemic treatment regimens.",
      "initial_approval_date": "2024-12-11",
      "initial_approval_url": "https://www.ema.europa.eu/en/documents/assessment-report/elahere-epar-public-assessment-report_en.pdf",
      "description": "The European Medicines Agency (EMA) has authorized mirvetuximab soravtansine for the treatment of adult patients with with folate receptor-alpha (FDalpha) positive, platinum-resistant high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who have received one to three prior systemic treatment regimens.",
      "raw_biomarkers": "folate receptor-alpha (FDalpha) positive",
      "raw_cancer_type": "high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer",
      "raw_therapeutics": "mirvetuximab soravtansine",
      "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.elahere",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Elahere (mirvetuximab soravtansine) [product information]. EMA.",
        "title": null,
        "aliases": [],
        "description": "AbbVie Deutschland GmbH & Co. KG. Elahere (mirvetuximab soravtansine) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/elahere-epar-product-information_en.pdf. Revised August 2025. Accessed September 8, 2025.",
        "urls": [
          "https://www.ema.europa.eu/en/medicines/human/EPAR/elahere",
          "https://www.ema.europa.eu/en/documents/product-information/elahere-epar-product-information_en.pdf"
        ],
        "doi": null,
        "pmid": null,
        "extensions": [
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            "name": "agent",
            "value": {
              "id": "ema",
              "type": "Agent",
              "agentType": "organization",
              "name": "European Medicines Agency",
              "description": "Regulatory agency that approves medicines for use in the European Union.",
              "extensions": [
                {
                  "name": "last_updated",
                  "value": "2025-10-01",
                  "description": ""
                },
                {
                  "name": "url",
                  "value": "https://www.ema.europa.eu/en/medicines",
                  "description": ""
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              ]
            },
            "description": "The organization that published this document."
          },
          {
            "name": "company",
            "value": "AbbVie Deutschland GmbH & Co. KG",
            "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
          },
          {
            "name": "drug_name_brand",
            "value": "Elahere",
            "description": "The brand name of the cancer drug, per this document. Only applicable to market authorization documents."
          },
          {
            "name": "drug_name_generic",
            "value": "mirvetuximab soravtansine",
            "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
          },
          {
            "name": "first_publication_date",
            "value": "2024-12-10",
            "description": "The publication date for the initial version of this document."
          },
          {
            "name": "identification_number",
            "value": null,
            "description": "Identification number used by the publishing organization."
          },
          {
            "name": "publication_date",
            "value": "2025-08-20",
            "description": "The publication date for the document."
          },
          {
            "name": "status",
            "value": "Active",
            "description": "Whether this document is Active or Deprecated within moalmanac-db."
          }
        ]
      }
    }
  ]
}