US FDA Doesn't Support Creating Ultra-Orphan Designation

Agency is already approving drugs for diseases with much smaller patient populations than the traditional rare disease, officials note.

FDA entrance sign 2016

The US FDA does not seem too interested in further subdividing the size of orphan diseases to create more incentives.

The so-called ultra-rare space, much smaller than a traditional rare disease, which FDA defines as affecting fewer than 200,000 people,...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Pink Sheet for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from US FDA

Former CBER Director Peter Marks Brings Genetic Medicines Street Cred To Lilly

 

FDA’s former CBER director is joining industry as senior VP of molecule discovery and head, infectious disease at Eli Lilly.

New US FDA Program Encouraging Domestic Manufacturing May Be ‘Very Selective’

 

Pharmaceutical manufacturers encouraged the FDA to consider including expansions and modifications of existing US drug facilities in the PreCheck program.

US FDA Independence Questioned At CDC Oversight Hearing

 

A Senate committee is investigating leadership changes at the US Centers for Disease Control and Prevention. While the primary focus is vaccine policy, the first hearing suggested the probe could raise questions about FDA independence.

Evita’s Mifepristone Approval Reignites Abortion Pill Controversy

 
• By 

An FDA approval of Evita Solutions' generic mifepristone 200mg tablets has reignited debate about the abortion pill, which Health and Human Services Secretary Robert F. Kennedy Jr. has indicated will be subject to a safety review.

More from Agency Leadership

New US FDA Program Encouraging Domestic Manufacturing May Be ‘Very Selective’

 

Pharmaceutical manufacturers encouraged the FDA to consider including expansions and modifications of existing US drug facilities in the PreCheck program.

US FDA Independence Questioned At CDC Oversight Hearing

 

A Senate committee is investigating leadership changes at the US Centers for Disease Control and Prevention. While the primary focus is vaccine policy, the first hearing suggested the probe could raise questions about FDA independence.

Evita’s Mifepristone Approval Reignites Abortion Pill Controversy

 
• By 

An FDA approval of Evita Solutions' generic mifepristone 200mg tablets has reignited debate about the abortion pill, which Health and Human Services Secretary Robert F. Kennedy Jr. has indicated will be subject to a safety review.