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Genentech’s Polivy (polatuzumab vedotin) Receives the US FDA’s Approval for Diffuse Large B-cell Lymphoma

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Genentech’s Polivy (polatuzumab vedotin) Receives the US FDA’s Approval for Diffuse Large B-cell Lymphoma

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  • The US FDA has approved Polivy in combination with Rituxan, cyclophosphamide, doxorubicin & prednisone (R-CHP) for adult patients before untreated DLBCL
  • The approval was based on the P-III trial (POLARIX) evaluating Polivy + R-CHP vs R-CHP in a ratio (1:1) in 1000 patients. The trial is being conducted in collaboration with LYSA & LYSARC
  • The results showed an improvement in PFS, a 27% reduction in risk of disease progression, relapse, or death. The safety profile was comparable, rates of grade 3-4 AEs (57.7% vs 57.5%), serious AEs (34.0% vs 30.6%), grade 5 AEs (3.0% vs 2.3%) & AEs leading to dose reduction (9.2% vs 13.0%). Polivy + bendamustine & Rituxan are currently approved in 80+ countries globally for r/r DLBCL

Ref: Businesswire | Image: Genentech

Related News:- Genentech Reports the US FDA Acceptance of sBLA for Polivy (polatuzumab vedotin-piiq) to Treat Diffuse Large B-Cell 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.

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