Fierce Healthcare March 15, 2024
Jon Gingrich

On Thursday, the Food and Drug Administration announced its approval of the first ever therapeutic treatment targeting metabolic dysfunction-associated steatohepatitis (MASH).

This represents a pivotal moment in healthcare and calls for a celebration.

This new therapeutic for advanced-stage liver disease is significant because, until now, diet and exercise were the only available treatment options.

It’s true this drug will be game-changing for physicians. More importantly, it will be life-changing for patients.

As we celebrate this milestone, we must ask ourselves: Are we truly prepared for when this drug hits the market?

The dire current reality

Nearly 1 in 4 Americans suffer from metabolic dysfunction–associated steatotic liver disease. Of that population, 20% have the more advanced disease form, MASH.

The more...

Today's Sponsors

LEK
ZeOmega

Today's Sponsor

LEK

 
Topics: Biotechnology, FDA, Govt Agencies, Pharma, Pharma / Biotech
Aviv Regev: The Revolution in Digital Biology
Global Inequities In Access To Drugs Costs Millions Of Lives Each Year
STAT+: New, serious safety risk related to MorphoSys’ cancer drug complicates, potentially threatens, Novartis acquisition
FDA Update for Week of April 22, 2024: Second Gene Therapy for Hemophilia B
Why Conflicts Of Interest May Not Be As Bad As You Think (And Besides We All Have Them!)

Share This Article