Social Science Research Network
NDA Approval Under FDCA Section 505(B)(1) Based On Effectiveness Data From One Clinical Trial
January 10, 2012
For new drug approval, the Food and Drug Administration (FDA) generally requires two or more clinical trials that demonstrate effectiveness. Notwithstanding, the Federal Food, Drug, and Cosmetic Act (FDCA) expressly authorizes FDA to approve drugs based on one trial with “confirmatory” evidence, and the Agency has issued guidance describing when only one trial is sufficient. To evaluate the frequency with which FDA approves new drugs based on only one trial, we researched the relevant statutory background and FDA guidance, and also reviewed new drug and biological product approvals since 1997. Out of 394 products approved from 1998 to 2011, we identified 30 products that were approved based on effectiveness data from one trial.
Contacts
Capabilities
Suggested News & Insights
Sidley Represents Immunovant in US$550 Million OfferingDecember 12, 2025BIOSECURE Act Included in the FY2026 National Defense Authorization ActDecember 12, 2025What the U.S.–UK Drug Pricing Agreement Reveals About How MFN Drug Policy Could Impact the UK and EUDecember 10, 2025U.S. FDA's Adoption of ICH E6(R3) Good Clinical Practice: Key Takeaways for Sponsors and InvestigatorsDecember 4, 2025Sidley Represents PayRange in Its Acquisition of KioSoftDecember 1, 2025Sidley Represents GE HealthCare in Its US$2.3 Billion Acquisition of InteleradNovember 20, 2025
- Stay Up To DateSubscribe to Sidley Publications
- Follow Sidley on Social MediaSocial Media Directory
