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...

    Key Potential Drug Launches in 2022

    Released July 22, 2021. Contains information like likelihood of approval (LOA) ratings and upcoming catalysts that are current as of April 2021.

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

    2020 Deal-Making Roundup

    Against a backdrop of unprecedented disruption, the biopharma and medtech industries reached incredible heights for deal-making activity during 2020.

    Topics Drug Review Coronavirus

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

    Q3 2021 Outlook Report

    What major drug catalysts and events can you expect to see in the months ahead? Download your free extract from the Q3 2021 Outlook Report and infographic to find out. Shape your strategy with your inside look at what’s to come.

    Topics Drug Review

;

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 ready to hear from you for a particular request or area of interest. Please do not hesitate to reach out and discuss.

Contact us for product technical and account support.

  • US Toll-Free   : +1 888 670 8900 
  • US Toll             : +1 212-600-3520
  • UK & Europe : +44 (0) 208 052 0700

Have an immediate and specific information need?

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