Logo

BMS' Inrebic (fedratinib) Receives EC's Approval for Patients with Newly Diagnosed and Previously Treated Myelofibrosis

Share this

BMS' Inrebic (fedratinib) Receives EC's Approval for Patients with Newly Diagnosed and Previously Treated Myelofibrosis

Shots:

  • The EC approval is based on JAKARTA and JAKARTA2 studies. The pivotal JAKARTA study involves assessing Inrebic (500mg) vs PBO in 289 patients with intermediate-2 or high-risk primary or secondary myelofibrosis with splenomegaly
  • The P-II JAKARTA 2 study involves assessing of Inrebic (400mg- qd) in 97 patients with intermediate or high-risk primary or secondary myelofibrosis with splenomegaly previously treated with ruxolitinib
  • Inrebic demonstrated spleen and symptom response in myelofibrosis patients where treatment with ruxolitinib has failed- who are intolerant to ruxolitinib or who are JAK inhibitor naïve. Inrebic is an oral kinase inhibitor with activity against JAK2 and FLT3

 ­ Ref: Businesswire | Image: BMS

Click here to­ read the full press release 

Senior Editor

This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com

Share this article on WhatsApp, LinkedIn and Twitter

Related News/Articles

Join the PharmaShots family of 12000+ subscribers

I accept the Terms and Conditions