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        "slug": "approved-immunotherapy-drugs-multi-year-total",
        "name": "Approved immunotherapy drugs (multi-year total)",
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        {
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        "slug": "biopharmaceutical-r-d-expenditure-multi-year-total",
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        {
          "slug": "pharmaceuticals",
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        "name": "United States",
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      "currency": "USD",
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        "bibtex": "@misc{phrma2024biopharmaceuticaladd4ew,\n  author       = {{PhRMA}},\n  title        = {Research \\& Development},\n  year         = {2024},\n  howpublished = {StatOrigin, https://statorigin.org},\n  url          = {https://statorigin.org/stat/stat_AA927K4APEG4WA76H7YWADD4EW},\n  note         = {Original source: https://phrma.org/policy-issues/research-development. Accessed September 17, 2026.}\n}"
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      "id": "stat_GJ0HSPRESAY30Y07N4XMBZF857",
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        "slug": "biosimilar-biological-product-approvals",
        "name": "Biosimilar biological product approvals",
        "definition": "Number of biosimilar biological products approved during the period."
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      "industry": [
        {
          "slug": "pharmaceuticals",
          "name": "Manufacture of basic pharmaceutical products and pharmaceutical preparations",
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      ],
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      "value": 18,
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        "org_url": "https://www.fda.gov",
        "org_tier": 1,
        "document_title": "CDER Brings Many Safe and Effective Therapies to Patients and Consumers in 2024",
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        "document_type": "press_release",
        "locator": "A Record Year for Biosimilar Approvals",
        "quote": "This milestone is due to CDER approving in 2024 a record total of 18 biosimilars for 8 reference products, more than any previous year.",
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        "apa": "U.S. Food and Drug Administration. (2024). CDER Brings Many Safe and Effective Therapies to Patients and Consumers in 2024. Retrieved September 17, 2026, from https://www.fda.gov/news-events/fda-voices/cder-brings-many-safe-and-effective-therapies-patients-and-consumers-2024. Via StatOrigin, https://statorigin.org/stat/stat_GJ0HSPRESAY30Y07N4XMBZF857",
        "bibtex": "@misc{fda2024biosimilarbzf857,\n  author       = {{U.S. Food and Drug Administration}},\n  title        = {CDER Brings Many Safe and Effective Therapies to Patients and Consumers in 2024},\n  year         = {2024},\n  howpublished = {StatOrigin, https://statorigin.org},\n  url          = {https://statorigin.org/stat/stat_GJ0HSPRESAY30Y07N4XMBZF857},\n  note         = {Original source: https://www.fda.gov/news-events/fda-voices/cder-brings-many-safe-and-effective-therapies-patients-and-consumers-2024. Accessed September 17, 2026.}\n}"
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        "slug": "botanical-drug-products-approved-as-prescription-drugs",
        "name": "Botanical drug products approved as prescription drugs",
        "definition": "Cumulative number of botanical drug products approved for marketing as prescription drugs through new drug applications."
      },
      "industry": [
        {
          "slug": "pharmaceuticals",
          "name": "Manufacture of basic pharmaceutical products and pharmaceutical preparations",
          "isic": "C21",
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        }
      ],
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        "code": "US",
        "name": "United States",
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        "start": "2026-09-03",
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        "org": "U.S. Food and Drug Administration",
        "org_short_name": "FDA",
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        "document_title": "FDA Seeks Public Input to Advance Development of Botanical Drug Products",
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        "document_type": "press_release",
        "locator": "FDA Seeks Public Input to Advance Development of Botanical Drug Products",
        "quote": "To date, four botanical products have been approved for marketing as prescription drugs through the FDA’s new drug application and biologics license application pathways.",
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        "accessed_at": "2026-09-17",
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        "apa": "U.S. Food and Drug Administration. (2026). FDA Seeks Public Input to Advance Development of Botanical Drug Products. Retrieved September 17, 2026, from https://www.fda.gov/news-events/press-announcements/fda-seeks-public-input-advance-development-botanical-drug-products. Via StatOrigin, https://statorigin.org/stat/stat_NRSYQY2AXZDY94AMEFRD5DCGKY",
        "bibtex": "@misc{fda2026botanical5dcgky,\n  author       = {{U.S. Food and Drug Administration}},\n  title        = {FDA Seeks Public Input to Advance Development of Botanical Drug Products},\n  year         = {2026},\n  howpublished = {StatOrigin, https://statorigin.org},\n  url          = {https://statorigin.org/stat/stat_NRSYQY2AXZDY94AMEFRD5DCGKY},\n  note         = {Original source: https://www.fda.gov/news-events/press-announcements/fda-seeks-public-input-advance-development-botanical-drug-products. Accessed September 17, 2026.}\n}"
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      "updated_at": "2026-09-17T07:16:01.811Z"
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        "slug": "covid-19-vaccines-and-therapeutics-spending-decline",
        "name": "COVID-19 vaccines and therapeutics spending decline",
        "definition": "Annual decline in spending on COVID-19 vaccines and antiviral therapeutics."
      },
      "industry": [
        {
          "slug": "pharmaceuticals",
          "name": "Manufacture of basic pharmaceutical products and pharmaceutical preparations",
          "isic": "C21",
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        }
      ],
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        "code": "US",
        "name": "United States",
        "type": "country"
      },
      "period": {
        "start": "2025-01-01",
        "end": "2025-12-31",
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      "value": 4,
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      "currency": "USD",
      "scale": "billion",
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        "org": "IQVIA Institute",
        "org_short_name": "IQVIA",
        "org_url": "https://www.iqvia.com",
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        "document_title": "U.S. Medicine Use Trends 2026",
        "document_url": "https://www.iqvia.com/insights/the-iqvia-institute/reports-and-publications/reports/us-medicine-use-trends-2026",
        "document_type": "press_release",
        "locator": "Other Findings",
        "quote": "COVID‑19 vaccines and therapeutics, which contributed to spending growth in 2024, declined by $4 billion in 2025.",
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        "accessed_at": "2026-09-15",
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        "url_status": "ok"
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        "apa": "IQVIA Institute. (2025). U.S. Medicine Use Trends 2026. Retrieved September 15, 2026, from https://www.iqvia.com/insights/the-iqvia-institute/reports-and-publications/reports/us-medicine-use-trends-2026. Via StatOrigin, https://statorigin.org/stat/stat_01M2KJ7XCF5037JCNPDKKT7NNA",
        "bibtex": "@misc{iqvia2025covidkt7nna,\n  author       = {{IQVIA Institute}},\n  title        = {U.S. Medicine Use Trends 2026},\n  year         = {2025},\n  howpublished = {StatOrigin, https://statorigin.org},\n  url          = {https://statorigin.org/stat/stat_01M2KJ7XCF5037JCNPDKKT7NNA},\n  note         = {Original source: https://www.iqvia.com/insights/the-iqvia-institute/reports-and-publications/reports/us-medicine-use-trends-2026. Accessed September 15, 2026.}\n}"
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      "updated_at": "2026-09-15T22:15:46.809Z"
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        "slug": "cell-and-gene-therapy-spending-share-by-geography",
        "name": "Cell and gene therapy spending share by geography",
        "definition": "Percentage of cell and gene therapy spending attributable to a given geography."
      },
      "industry": [
        {
          "slug": "pharmaceuticals",
          "name": "Manufacture of basic pharmaceutical products and pharmaceutical preparations",
          "isic": "C21",
          "is_primary": true
        }
      ],
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        "code": "US",
        "name": "United States",
        "type": "country"
      },
      "period": {
        "start": "2023-01-01",
        "end": "2023-12-31",
        "type": "year"
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      "value": 62,
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      "scale": "1",
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        "org": "IQVIA Institute",
        "org_short_name": "IQVIA",
        "org_url": "https://www.iqvia.com",
        "org_tier": 3,
        "document_title": "Strengthening Pathways for Cell and Gene Therapies: Current State and Future Scenarios",
        "document_url": "https://www.iqvia.com/insights/the-iqvia-institute/reports-and-publications/reports/strengthening-pathways-for-cell-and-gene-therapies",
        "document_type": "press_release",
        "locator": "Global cell and gene therapy spending and share by geography",
        "quote": "A majority (62%) of this spending is attributable to U.S. sales, compared to just 38% coming from other geographies.",
        "published_date": null,
        "accessed_at": "2026-09-15",
        "license": "see-source",
        "url_status": "ok"
      },
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      "verified_by": "seed:auto-extract-v1",
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        "apa": "IQVIA Institute. (2023). Strengthening Pathways for Cell and Gene Therapies: Current State and Future Scenarios. Retrieved September 15, 2026, from https://www.iqvia.com/insights/the-iqvia-institute/reports-and-publications/reports/strengthening-pathways-for-cell-and-gene-therapies. Via StatOrigin, https://statorigin.org/stat/stat_01M2KJ7XCF5037JCNPDKKT7NNX",
        "bibtex": "@misc{iqvia2023cellkt7nnx,\n  author       = {{IQVIA Institute}},\n  title        = {Strengthening Pathways for Cell and Gene Therapies: Current State and Future Scenarios},\n  year         = {2023},\n  howpublished = {StatOrigin, https://statorigin.org},\n  url          = {https://statorigin.org/stat/stat_01M2KJ7XCF5037JCNPDKKT7NNX},\n  note         = {Original source: https://www.iqvia.com/insights/the-iqvia-institute/reports-and-publications/reports/strengthening-pathways-for-cell-and-gene-therapies. Accessed September 15, 2026.}\n}"
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      "indicator": {
        "slug": "clinical-development-regulatory-approval-rate",
        "name": "Clinical development regulatory approval rate",
        "definition": "Proportion of drug candidates entering clinical trials that successfully receive regulatory marketing authorization."
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      "industry": [
        {
          "slug": "pharmaceuticals",
          "name": "Manufacture of basic pharmaceutical products and pharmaceutical preparations",
          "isic": "C21",
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        }
      ],
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        "code": "US",
        "name": "United States",
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        "start": "2025-01-01",
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        "org": "PhRMA",
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        "org_tier": 2,
        "document_title": "Research & Development",
        "document_url": "https://phrma.org/policy-issues/research-development",
        "document_type": "press_release",
        "locator": "Progress toward New Medicines and Vaccines",
        "quote": "Only 12% of new molecular entities that enter clinical trials eventually receive U.S. Food and Drug Administration (FDA) approval.",
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        "accessed_at": "2026-09-17",
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      "citation": {
        "apa": "PhRMA. (2025). Research & Development. Retrieved September 17, 2026, from https://phrma.org/policy-issues/research-development. Via StatOrigin, https://statorigin.org/stat/stat_V2J1XACMRQE968NSWN5E8TT1Q5",
        "bibtex": "@misc{phrma2025clinical8tt1q5,\n  author       = {{PhRMA}},\n  title        = {Research \\& Development},\n  year         = {2025},\n  howpublished = {StatOrigin, https://statorigin.org},\n  url          = {https://statorigin.org/stat/stat_V2J1XACMRQE968NSWN5E8TT1Q5},\n  note         = {Original source: https://phrma.org/policy-issues/research-development. Accessed September 17, 2026.}\n}"
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      "id": "stat_01M2KJ7XCG3Y4BJ2059JBJMGCT",
      "url": "https://statorigin.org/stat/stat_01M2KJ7XCG3Y4BJ2059JBJMGCT",
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        "slug": "clinical-trial-country-use-share",
        "name": "Clinical trial country use share",
        "definition": "Percentage of total clinical trial country uses accounted for by a given region."
      },
      "industry": [
        {
          "slug": "pharmaceuticals",
          "name": "Manufacture of basic pharmaceutical products and pharmaceutical preparations",
          "isic": "C21",
          "is_primary": true
        }
      ],
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        "code": "US",
        "name": "United States",
        "type": "country"
      },
      "period": {
        "start": "2021-01-01",
        "end": "2023-12-31",
        "type": "year"
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      "scale": "1",
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        "org": "IQVIA Institute",
        "org_short_name": "IQVIA",
        "org_url": "https://www.iqvia.com",
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        "document_url": "https://www.iqvia.com/insights/the-iqvia-institute/reports-and-publications/reports/rethinking-clinical-trial-country-prioritization",
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        "locator": "Country utilization is heavily consolidated in U.S., China and Western European countries",
        "quote": "The top 10 most used countries account for 58% of the total average pipeline country use, with the United States and China responsible for 16% and 13%, respectively, of total country-uses for trials started in the 2021–2023 timeframe.",
        "published_date": null,
        "accessed_at": "2026-09-15",
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        "apa": "IQVIA Institute. (2023). Rethinking Clinical Trial Country Prioritization. Retrieved September 15, 2026, from https://www.iqvia.com/insights/the-iqvia-institute/reports-and-publications/reports/rethinking-clinical-trial-country-prioritization. Via StatOrigin, https://statorigin.org/stat/stat_01M2KJ7XCG3Y4BJ2059JBJMGCT",
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        "bibtex": "@misc{europeancommissi2025healthb52tzf,\n  author       = {{European Commission}},\n  title        = {The 2025 EU Industrial R\\&D Investment Scoreboard},\n  year         = {2025},\n  howpublished = {StatOrigin, https://statorigin.org},\n  url          = {https://statorigin.org/stat/stat_T9AE55AFXEF16A7X4A2CB52TZF},\n  note         = {Original source: https://joint-research-centre.ec.europa.eu/jrc-news-and-updates/2025-eu-industrial-rd-investment-scoreboard-2025-12-22\\_en. Accessed September 17, 2026.}\n}"
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          "slug": "pharmaceuticals",
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          "slug": "pharmaceuticals",
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