Sorrento's Partner Mabpharm Files NDA to the NMPA for Infliximab Biosimilar in China
Shots:
- Mabpharm files Infliximab Biosimilar’s NDA to the NMPA based on the trial evaluating Infliximab Biosimilar vs Infliximab and has used CHO expression system which resulted in safety results and lower immunogenicity
- Sorrento plans to file BLA for Infliximab Biosimilar in the US by the end of 2020. Sorrento signed a worldwide license agreement with Mabpharm- and has global rights to Mabpharm Infliximab biobetter Ab outside of China
- Remicade (Infliximab) is a mAb works as a tumor necrosis factor inhibitors (TNFs) targeted for RA- CD- UC- AS (a type of spinal arthritis)- PsA- and the red- scaly skin patches of plaque psoriasis. Sorrento is also developing Resiniferatoxin (“RTX”) a P-Ib candidate for terminal cancer and osteoarthritis patients
Click here to read full press release/ article | Ref: GlobeNewswire | Image: Behance
Tags
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