Logo

Genentech’s Glofitamab Receives BLA & Priority Review from the US FDA to Treat r/r Large B-Cell Lymphoma

Share this
Genentech

Genentech’s Glofitamab Receives BLA & Priority Review from the US FDA to Treat r/r Large B-Cell Lymphoma

Shots:

  • The BLA submission was based on the P-I/II clinical trial evaluating glofitamab in 2L+ LBCL patients (n=155) refractory to their most recent therapy (85.1%) or failed CAR T-cell therapy (33.1%)
  • The results from the study depicted a CR in 40.0% of the patients (73.1% showed continued response @12mos. & mDoR was 18.4mos.), OR in 51.6%, median follow-up time of 13.4mos. The earlier cut-off data depicted a CR of 11.5mos. & 12mos. post-treatment 61% of patients maintained a CR, 92.6% remained progression-free
  • Glofitamab is a CD20xCD3 T-cell engaging bispecific Ab. and is being assessed in P-III combination study (STARGLO) in patients with DLBCL

Ref: Businesswire | Image: Genentech

Related News:- Genentech’s Lunsumio (mosunetuzumab-axgb) Receives the US FDA’s Approval for Relapsed or Refractory Follicular Lymphoma

Click here to­ read the full press release 

Senior Editor

Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

Share this article on WhatsApp, LinkedIn and Twitter

Join the PharmaShots family of 12000+ subscribers

I accept the Terms and Conditions