BMS's Reblozyl Data Supports Adding Less Severe Patients To Label

Adding non-transfusion-dependent anemia patients to the Reblozyl label is a key strategy for the product, which BMS expects to reach $4bn in annual sales.

Bristol-Myers-Squib_685347493_1200.jpg
BMS and partner Acceleron hope to move Reblozyl into earlier-stage anemia

Bristol Myers Squibb Company presented data on 11 June showing that its erythroid maturation drug Reblozyl can increase hemoglobin in 77% of patients with non-transfusion-dependent (NTD) beta thalassemia compared to zero on placebo, perhaps positioning the product to add a third indication to its label.

Although the Phase II BEYOND study readout is unlikely to serve as pivotal data, Noah Berkowitz, BMS’s senior vice president...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Scrip 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 Clinical Trials

Ionis’s Olezarsen Data Meet Multiple Marks In Blockbuster sHTG Indication

 
• By 

Phase III CORE and CORE2 results presented at the AHA meeting in severe hypertriglyceridemia showed durable triglyceride lowering and reductions in acute pancreatitis across patient subgroups, supporting expansion of Tryngolza (olezarsen) into a second, larger indication.

Amgen’s ‘Stunning’ VESALIUS Results Could Push Repatha Into The Mainstream

 
• By 

Cardiologists know PCSK9 inhibition is a powerful LDL-lowering tool and now Amgen’s VESALIUS data show it may be worth adding to the primary care physician’s toolbox for prevention of high-risk patients’ first major cardiovascular events.

Lilly’s Eloralintide Success Sets Bar For Amylin Rivals

 

The US pharma giant may have a best-in-class amylin agonist to go with incretin blockbuster Zepbound, but challengers could still go one better on safety and tolerability.

Centessa’s Sleep Disorder Drug Shows Broad Potential But Faces Tough Competition

 

Pivotal data next year will be key for the early-stage biotech as analysts remain divided on ORX750's potential.

More from R&D

Aurobindo On Easier US Biosimilar Pathway, Zentiva Miss And Deal Strategy

 
• By 

Do US FDA’s efforts at simplifying the biosimilar pathway create more competition and threaten Aurobindo Pharma's return on investments? Management speaks on this, biosimilar filing plans and deal strategy at the Q2 FY26 earnings call

Korean Biosimilars Giants Step Up Race To Become Innovators

 
• By 

South Korea’s two biosimilars giants have laid out differing strategies to pursue innovative drug R&D, although both are positioning ADCs as a core focus.

Lilly Plans Phase III Trials After Positive Results From Amylin Drug Eloralintide

 

The drugmaker presented positive data from its Phase II study at ObesityWeek that help validate the amylin class overall, which includes more than a dozen entrants.