Shots:

• SciClone has submitted the BLA for Danyelza to treat pediatric patients aged >1 yr. and adult patients with r/r high-risk neuroblastoma to NMPA in China
• If approved- the therapy will be available in the China imminently. The therapy was approved under accelerated approval based on ORR and DoR while the continued approval for the indication may be contingent upon verification and description of clinical benefits in a confirmatory trial
• MSK’s researchers have developed the therapy which is exclusively licensed to Y-mAbs. Following the licensing arrangement- MSK has institutional financial interests in the product

  Ref: Globe Newswire | Image: Y-mAbs