skip to main content
Close Icon We use cookies to improve your website experience.  To learn about our use of cookies and how you can manage your cookie settings, please see our Cookie Policy.  By continuing to use the website, you consent to our use of cookies.
Global Search Configuration

In August, Forbes’ reporter Matthew Herper penned an article using data from the BioMedTracker database highlighting the unprecedented rate of approval by the U.S. Food & Drug Administration (FDA) for new molecular entity (NME) applications in recent years. In this follow-up analysis we compared how the FDA has been approving NME applications in relation to how advisory committees (AdComms) have voted on their approvability. We decided to compare these two different bodies as it shows the opinions of a group that can most closely be considered peer to the FDA when it comes to reviewing drug applications in the United States. AdComms are convened by the FDA to provide independent advice from outside experts on the quality of drug applications and vote on whether the application should be approved or not. There are a few things to keep in mind when looking at this analysis; there is a provision in PDUFA IV that requires AdComm meetings be held to review NME applications, the FDA usually doesn’t convene AdComms for non-NME applications except in rare instances, and the FDA is not bound by the voting outcome of the AdComm.

The graph below shows results for all FDA approval decisions for NME filings that were preceded by an AdComm vote.

 FDA Decisions following Advisory Committee Recommendations

Source: BioMedTracker’s AdComm Insight

The blue bars represent the total number of FDA decisions in a given year that were also reviewed by an AdComm. The red bars show how many of those applications an AdComm voted in favor of approval for, and the gray bars show the total number of FDA approvals granted following an AdComm meeting.

One would expect that if the FDA were seeing higher quality NME applications then positive AdComm opinions would continue to outpace approvals. That is however not the case and the conclusion from this analysis is that the FDA is becoming more lenient when it comes to approving new drugs. All the way back through 2006, the FDA has been more conservative than their AdComm peers when reviewing NME applications. Only in 2006 and 2011 did they approve as many NMEs as AdComms deemed fit for approval. In 2014 that trend reversed and the FDA became more liberal than the AdComm opinions and approved more drugs than the respective committees deemed fit for approval. That trend has continued thus far into 2015, but with four scheduled AdComm meetings planned it remains to be seen if that trend will hold.

Read also

  • Biomedtracker: see the drug development process through anal...

    COVID-19 Infographic

    Access the infographic below which explores the number of treatment drugs for COVID-19 currently in clinical trials or in development, events including progress updates, partnerships, regulatory and trial announcements etc, and the number of articles published on COVID-19 as of March 3, 2020. This data has been tracked and reported via Informa Pharma Intelligence’s clinical, regulatory and commercial data and analytics, and news and insight tools including Biomedtracker, Trialtrove, Pharmaprojects, Scrip, Pink Sheet, Medtech Insight, and Generics Bulletin etc.

    Topics Coronavirus

  • Biomedtracker: see the drug development process through anal...

    Biomedtracker Potential Pivots in 2020

    In this infographic, we provide insight into key trials that are expecting developments in the approval process.

    Topics

  • Biomedtracker: see the drug development process through anal...

    2020 Early Outlook Webinar

    By Michael Haydock

    Anticipate the biggest, most impactful expected catalysts of early 2020 with the guidance and insights from Pharma Intelligence. Building off Biomedtracker’s Early 2020 Outlook report, our live webinar will include market context for these upcoming milestones and additional insights from Datamonitor Healthcare’s Therapeutic Area Directors.

    Topics FDA

;

Next steps

Getting a demo tailored to your needs is the best way to see how our solutions will help you gain an advantage.

Request live demo now:

Our team is always happy to hear from you. Please call us at:

  • US Toll-Free  : +1 888 670 8900
  • US Toll           : +1 908 547 2200
  • UK & Europe : +44 (20) 337 73737
  • Australia        : +61 2 8705 6907
  • Japan              : +81 3 6273 4260

Or please submit your inquiry via the form so that we can provide you the best possible customer service.

Have an immediate and specific information need?

Browse and buy from 1000s of analysis and research reports now: