European Commission approves Onureg for certain AML subtypes

Share on facebook
Share on twitter
Share on linkedin
Share on email
Share on print

The European Commission has approved Onureg (azacitidine tablets)as the first and only once-daily, frontline oral maintenance therapy in the EU for patients with a broad range of acute myeloid leukemia subtypes. 

While many patients with AML achieve remission with induction therapy, about 50% of patients relapse within one year. In the pivotal QUAZAR AML-001 study, Onureg significantly improved overall survival and relapse-free survival in patients with AML, reinforcing its clinical benefit and role in the treatment paradigm for patients with this common acute leukemia.

Onureg is sponsored by Bristol Myers Squibb.

Table of Contents

YOU MAY BE INTERESTED IN

Growing up in inner-city Detroit, Otis Brawley had a thriving community made up of his parents, Jesuit priests, friends, and neighbors encouraging him that he could do anything he put his mind to. 
On Feb. 3, the House of Representatives passed the Senate Amendment to H.R. 7148, the Consolidated Appropriations Act, 2026, by a vote of 217 to 214. Later that day, President Donald Trump signed the bill into law, officially ending the brief partial government shutdown that began on Jan. 31. 

Never miss an issue!

Get alerts for our award-winning coverage in your inbox.

Login