Skip to Primary Navigation

FDA announces new regulatory framework for ultra-rare disease therapies

A photo of the seal of the US Food and Drug Administration on a sign in front of its headquarters.
Photo: Sarah Silbiger/Getty Images

The guidance will enable the agency to accelerate approval on new treatments for diseases affecting fewer than 1 in 50,000 people.

The US Food and Drug Administration (FDA) has issued draft guidance for a new regulatory framework for drug sponsors seeking approval for targeted individualized therapies for ultra-rare diseases.

The so-called plausible mechanism framework aims to reduce hurdles for individualized medicines designed for patients with diseases so uncommon that it may

Get full access, free for a month

Start your 28-day free trial to continue reading and access
all content on GRIP – no payment details required.

What’s included:

  • Every new article, plus our 5,000+ archive
  • Daily regulatory insight and guidance
  • Exclusive interviews and in-depth analysis
  • Coverage of industry-leading events and conferences
  • All podcasts and videos, featuring industry experts
  • The full set of Rules Navigator tools
  • An ad-free experience