{
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    "timestamp_received": "2026-11-09T16:12:46.276809Z",
    "timestamp_returned": "2026-11-09T16:12:46.278380Z",
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    "name": "Molecular Oncology Almanac",
    "license": "GPL-2.0",
    "release": "draft",
    "url": "https://moalmanac.org",
    "last_updated": "2026-10-08"
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  "data": [
    {
      "id": "ind:fda:jemperli:0",
      "type": "Indication",
      "description": "JEMPERLI is a programmed death receptor-1 (PD-1)-blocking antibody indicated in combination with carboplatin and paclitaxel, followed by JEMPERLI as a single agent for the treatment of adult patients with primary advanced or recurrent endometrial cancer that is mismatch repair deficient (dMMR), as determined by an FDA-approved test, or microstallite instability-high (MSI-H).",
      "contributions": [
        {
          "id": "ctrb:vanallenlab:2024-10-30:0",
          "type": "Contribution",
          "description": "Initial access of FDA approvals",
          "date": "2024-10-30",
          "contributor": {
            "id": "agent:user:vanallenlab",
            "type": "Agent",
            "agentType": "contributor",
            "name": "Van Allen lab",
            "description": "Van Allen lab, Dana-Farber Cancer Institute"
          }
        },
        {
          "id": "ctrb:fda:2023-07-31:0",
          "type": "Contribution",
          "description": "Indication received traditional approval.",
          "date": "2023-07-31",
          "contributor": {
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            "type": "Agent",
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            "description": "Regulatory agency that approves drugs for use in the United States."
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      "reportedIn": [
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          "id": "doc:fda:jemperli",
          "type": "Document",
          "documentType": "Regulatory approval",
          "name": "Jemperli (dostarlimab) [package insert]. FDA.",
          "title": null,
          "aliases": [],
          "description": "GlaxoSmithKline LLC. Jemperli (dostarlimab) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/761174s010lbl.pdf. Revised March 2024. Accessed October 30, 2024.",
          "urls": [
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            "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=761174"
          ],
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          "pmid": null,
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              "description": "The organization that published this document."
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            {
              "name": "company",
              "value": "GlaxoSmithKline LLC.",
              "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
            },
            {
              "name": "drug_name_brand",
              "value": "Jemperli",
              "description": "The brand name of the cancer drug, per this document. Only applicable to market authorization documents."
            },
            {
              "name": "drug_name_generic",
              "value": "dostarlimab",
              "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": null,
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              "description": "The publication date for the document."
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              "value": "BLA761174",
              "description": "Identifier assigned by the regulatory agency, such as an FDA application number (e.g. NDA208716, BLA125427) or an EMA product number (e.g. EMEA/H/C/006184)."
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        {
          "id": "doc:fda:jemperli:2023-07-31",
          "type": "Document",
          "documentType": "Regulatory approval",
          "name": "Jemperli (dostarlimab) [package insert]. FDA.",
          "title": null,
          "aliases": [],
          "description": "GlaxoSmithKline LLC. Jemperli (dostarlimab) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/761174s006lbl.pdf. Revised July 2023. Accessed October 6, 2026.",
          "urls": [
            "https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/761174s006lbl.pdf",
            "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=761174"
          ],
          "doi": null,
          "pmid": null,
          "extensions": [
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              "name": "agent",
              "value": {
                "id": "agent:org:fda",
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                "name": "Food and Drug Administration",
                "description": "Regulatory agency that approves drugs for use in the United States."
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              "description": "The organization that published this document."
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            {
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              "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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              "description": "The brand name of the cancer drug, per this document. Only applicable to market authorization documents."
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            {
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              "value": "dostarlimab",
              "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": null,
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            {
              "name": "publication_date",
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              "description": "The publication date for the document."
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          "value": "Approved",
          "description": "Current approval status."
        },
        {
          "name": "statement description",
          "value": "The U.S. Food and Drug Administration granted approval to dostarlimab in combination with carboplatin and paclitaxel, followed by dostarlimab as a single agent, for the treatment of adult patients with primary advanced or recurrent endometrial cancer that is mismatch repair deficient (dMMR), as determined by an FDA-approved test, or microstallite instability-high (MSI-H).",
          "description": "The description text for all Statements derived from this Indication."
        }
      ]
    }
  ]
}