Novo Nordisk Receives BLA Approval for Esperoct (turoctocog alfa pegol, N8-GP) for Patients with Haemophilia A
Shots:
- The BLA approval is based on the trial assessing Esperoct (turoctocog alfa pegol, N8-GP) in 270 patients with previously treated people (PTPs) with severe haemophilia A
- The study resulted in maintanince of low median ABR of 1.18, efficacious in treatment & control of bleeding episodes, perioperative management and was well tolerated with no safety concerns observed
- Esperoct (turoctocog alfa pegol, N8-GP) is an extended half-life factor VIII molecule indicated as a replacement therapy in people with haemophilia A and will be marketed in US in 2020
Click here to read full press release/ article| Ref: Novo Nordisk | Image: Azernews