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Despite Criticism Of The FDA Review Process, New Cancer Drugs Reach Patients Sooner In The United States Than In Europe
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Despite Criticism Of The FDA Review Process, New Cancer Drugs Reach Patients Sooner In The United States Than In Europe (2011)Despite Criticism Of The FDA Review Proce…Reputation and Power (2014)Reputation and PowerPharmaceutical Innovation in the 21st Century: New Drug Approvals in the First Decade, 2000–2009 (2010)Pharmaceutical Innovation in …Economics of New Oncology Drug Development (2007)Economics of New Oncology Dru…Reimbursement for Cancer Treatment: Coverage of Off-Label Drug Indications (2006)Reimbursement for Cancer Trea…Comparison of Cancer-Related Spending and Mortality Rates in the US vs 21 High-Income Countries (2022)Comparison of Cancer-Related …Patient-Reported Outcomes Labeling for Products Approved by the Office of Hematology and Oncology Products of the US Food and Drug Administration (2010-2014) (2016)Patient-Reported Outcomes Lab…Use of the conditional marketing authorization pathway for oncology medicines in Europe (2015)Use of the conditional market…Balancing early market access to new drugs with the need for benefit/risk data: a mounting dilemma (2008)Diagnosing the decline in pharmaceutical R&D efficiency (2012)From adaptive licensing to adaptive pathways: Delivering a flexible life‐span approach to bring new drugs to patients (2015)Characteristics and follow‐up of postmarketing studies of conditionally authorized medicines in the EU (2016)Cost of innovation in the pharmaceutical industry (1991)The price of innovation: new estimates of drug development costs (2003)Estimating The Cost Of New Drug Development: Is It Really $802 Million? (2006)Incentives for orphan drug research and development in the United States (2008)The High Cost of Cancer Drugs and What We Can Do About It (2012)Estimating the cost of vaccine development against epidemic infectious diseases: a cost minimisation study (2018)The cost of biopharmaceutical R&D: is biotech different? (2007)Lessons from 60 years of pharmaceutical innovation (2009)Trends in Risks Associated With New Drug Development: Success Rates for Investigational Drugs (2010)Clinical development success rates for investigational drugs (2014)Scientific and Regulatory Reasons for Delay and Denial of FDA Approval of Initial Applications for New Drugs, 2000-2012 (2014)Changing R&D models in research-based pharmaceutical companies (2016)Reputation and Public Administration (2011)6 SMALL STATES IN WORLD MARKETS Industrial Policy in Europe (2012)Assessing the Gold Standard — Lessons from the History of RCTs (2016)Organizing for Crisis Management: Building Governance Capacity and Legitimacy (2016)A Review of Patient-Reported Outcome Labels in the United States: 2006 to 2010 (2012)Assessment of PRO Label Claims Granted by the FDA as Compared to the EMA (2006–2010) (2013)Patient-Reported Outcomes in Cancer Drug Development and US Regulatory Review (2015)The Spectrum of Functional Rating Scales in Neurology Clinical Trials (2016)Financial Hardships Experienced by Cancer Survivors: A Systematic Review (2016)Health Care Spending in the United States and Other High-Income Countries (2018)US Health Care Spending by Payer and Health Condition, 1996-2016 (2020)Health technology assessment for cancer medicines across the G7 countries and Oceania: an international, cross-sectional study (2023)Steady Increase In Prices For Oral Anticancer Drugs After Market Launch Suggests A Lack Of Competitive Pressure (2016)Investigating the landscape of US orphan product approvals (2018)
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References

  • 2014Reputation and Power862 cited
  • 2007Economics of New Oncology Drug Development348 cited
  • 2010Pharmaceutical Innovation in the 21st Century: New Drug Approvals in the First Decade, 2000–2009329 cited
  • 2006Reimbursement for Cancer Treatment: Coverage of Off-Label Drug Indications81 cited

Cited by

  • 2022Comparison of Cancer-Related Spending and Mortality Rates in the US vs 21 High-Income Countries62 cited
  • 2016Patient-Reported Outcomes Labeling for Products Approved by the Office of Hematology and Oncology Products of the US Food and Drug Administration (2010-2014)58 cited
  • 2015Use of the conditional marketing authorization pathway for oncology medicines in Europe57 cited

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