Register Now: From Clinical to Commercial: Accelerating ADC Late-Stage Development with Technology Innovation and Integrated Platform
|Articles|January 11, 2021

WuXi STA Supports Approval from NMPA for Orelabrutinib from InnoCare

WuXi STA served as the marketing authorization holder (MAH) and offered end-to-end support, including drug substance, amorphous solid dispersion, tablet, and packaging for the product.

STA Pharmaceutical (WuXi STA), a WuXi AppTec Company, announced on Jan. 6, 2020 that its partner, InnoCare, a biopharmaceutical company based in China, has received approval by the National Medical Products Administration of China (NMPA) for orelabrutinib, a Bruton Tyrosine Kinase inhibitor for the treatment of cancer and autoimmune diseases.

According to a WuXi company press release, WuXi STA served as the marketing authorization holder (MAH) and offered end-to-end support, including drug substance, amorphous solid dispersion, tablet, and packaging for the product. Additionally, WuXi STA’s facilities were inspected throughout September and October of 2020 and successfully passed the pre-approval inspection (PAI) by NMPA for orelabrutinib.

“We are excited that [o]relabrutinib was approved by NMPA,” said Dr. Jasmine Cui, InnoCare co-founder, chairman, and CEO, in the press release. “As our important partner of this innovative drug, WuXi STA has provided CMC [chemistry, manufacturing, and controls] support from clinical trials to commercialization, and successfully passed PAI for Orelabrutinib. We look forward to working with WuXi STA to address more unmet medical needs.”

“We sincerely congratulate our partner InnoCare on the approval of [o]relabrutinib,” added Dr. Minzhang Chen, CEO of WuXi STA, in the press release. “The successful PAI is the result of close team collaboration between WuXi STA and our partner InnoCare.”

Source: WuXi STA


Related to this article

The BioPharm Brief: An AI-Designed Multibody ADC Enters the Clinic, Blackstone Backs Pfizer’s Monthly GLP-1, and enGene Readies a Bladder Cancer BLA
FDA clears the IND for Biolojic Design’s BD200, an AI-designed Trop2/Nectin-4 multibody ADC; Blackstone Life Sciences agrees to provide Pfizer up to $1.5 billion to develop its monthly GLP-1 receptor agonist berobenatide; and enGene Therapeutics plans a year-end BLA for detalimogene voraplasmid in BCG-unresponsive non-muscle invasive bladder cancer.