{
  "meta": {
    "data_length": 1,
    "message": "Indication id ind:fda:opdivo:2 retrieved successfully",
    "request_url": "http://api.moalmanac.org/indications?indication_id=ind%3Afda%3Aopdivo%3A2",
    "status": "success",
    "status_code": 200,
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    "timestamp_received": "2026-09-25T00:11:56.811908+00:00Z",
    "timestamp_returned": "2026-09-25T00:11:56.813504+00:00Z",
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    "name": "Molecular Oncology Almanac",
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    "release": "draft",
    "url": "https://dev.moalmanac.org",
    "last_updated": "2026-08-02"
  },
  "data": [
    {
      "id": "ind:fda:opdivo:2",
      "type": "Indication",
      "description": "OPDIVO is a programmed death receptor-1 (PD-1)-blocking antibody indicated for the treatment of adult patients with metastatic or recurrent non-small cell lung cancer with no EGFR or ALK genomic tumor aberrations as first-line treatment, in combination with ipilimumab and 2 cycles of platinum-doublet chemotherapy.",
      "contributions": [
        {
          "id": "ctrb:fda:2025-05-26:0",
          "type": "Contribution",
          "description": "Indication received traditional approval.",
          "date": "2025-05-26",
          "contributor": {
            "id": "agent:org:fda",
            "type": "Agent",
            "agentType": "organization",
            "name": "Food and Drug Administration",
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          "contributor": {
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            "type": "Agent",
            "agentType": "contributor",
            "name": "Van Allen lab",
            "description": "Van Allen lab, Dana-Farber Cancer Institute"
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        {
          "id": "ctrb:fda:2020-05-26:0",
          "type": "Contribution",
          "description": "Indication received accelerated approval.",
          "date": "2020-05-26",
          "contributor": {
            "id": "agent:org:fda",
            "type": "Agent",
            "agentType": "organization",
            "name": "Food and Drug Administration",
            "description": "Regulatory agency that approves drugs for use in the United States."
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      "reportedIn": [
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          "id": "doc:fda:opdivo",
          "type": "Document",
          "documentType": "Regulatory approval",
          "name": "Opdivo (nivolumab) [package insert]. FDA.",
          "title": null,
          "aliases": [],
          "description": "Bristol-Myers Squibb Company. Opdivo (nivolumab) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/125554s129lbl.pdf. Revised April 2025. Accessed April 30, 2025.",
          "urls": [
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            "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=125554"
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              "description": "The organization that published this document."
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            {
              "name": "company",
              "value": "Bristol-Myers Squibb Company.",
              "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
            },
            {
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              "value": "Opdivo",
              "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": "nivolumab",
              "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": "2014-12-22",
              "description": "The publication date for the initial version of this document."
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            },
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              "value": "2025-04-11",
              "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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      "extensions": [
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          "name": "status",
          "value": "Approved",
          "description": "Current approval status."
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}