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    "timestamp_received": "2026-04-23T23:24:20.098048+00:00Z",
    "timestamp_returned": "2026-04-23T23:24:20.101964+00:00Z",
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    "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:fda.vizimpro:0",
      "indication": "VIZIMPRO is a kinase inhibitor indicated for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletion or exon 21 L858R substitution mutations as detected by an FDA-approved test.",
      "initial_approval_date": "2018-09-27",
      "initial_approval_url": "https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/211288s000lbl.pdf",
      "description": "The U.S. Food and Drug Administration granted approval to dacomitinib for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletion or exon 21 L858R substitution mutations, as detected by an FDA-approved test.",
      "raw_biomarkers": "EGFR exon 19 deletion or exon 21 L858R substitution mutations",
      "raw_cancer_type": "metastatic non-small cell lung cancer",
      "raw_therapeutics": "Vizimpro (dacomitinib)",
      "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:fda.vizimpro",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Vizimpro (dacomitinib) [package insert]. FDA.",
        "title": null,
        "aliases": [],
        "description": "Pfizer, Inc. Vizimpro (dacomitinib) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/211288s003lbl.pdf. Revised December 2020. Accessed October 30, 2024.",
        "urls": [
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        "pmid": null,
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                  "description": ""
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            "description": "The organization that published this document."
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          {
            "name": "company",
            "value": "Pfizer, Inc.",
            "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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            "value": "Vizimpro",
            "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": "dacomitinib",
            "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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            "value": null,
            "description": "The publication date for the initial version of this document."
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            "value": "2020-12-18",
            "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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  ]
}