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    {
      "id": "ind:fda.augtyro:0",
      "indication": "AUGTYRO is a kinase inhibitor indicated for the treatment of adult patients with locally advanced or metastatic ROS1-positive non-small cell lung cancer (NSCLC).",
      "initial_approval_date": "2023-11-15",
      "initial_approval_url": "https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/218213s000lbl.pdf",
      "description": "The U.S. Food and Drug Administration granted approval to repotrectinib for the treatment of adult patients with locally advanced or metastatic ROS1-positive non-small cell lung cancer (NSCLC).",
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      "raw_therapeutics": "Augtyro (repotrectinib)",
      "icd10": null,
      "regimen_code": null,
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      "date_accelerated_approval": null,
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        "type": "Document",
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        "name": "Augtyro (repotrectinib) [package insert]. FDA.",
        "title": null,
        "aliases": [],
        "description": "Bristol-Myers Squibb. Augtyro (repotrectinib) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/218213s001lbl.pdf. Revised June 2024. Accessed October 30, 2024.",
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}