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Genentech's Tiragolumab + Tecentriq Receive the US FDA's Breakthrough Therapy Designation for PD-L1-High Non-Small Cell Lung Cancer

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Genentech's Tiragolumab + Tecentriq Receive the US FDA's Breakthrough Therapy Designation for PD-L1-High Non-Small Cell Lung Cancer

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  • The BTD is based on P-II CITYSCAPE study assessing Tiragolumab + Tecentriq vs Tecentriq + PBO as a 1L treatment of 135 patients in a ratio (1:1) with LA unresectable metastatic NSCLC whose tumors have high PD-L1 expression with no EGFR
  • Result: improvement in ORR (37% vs 21%); reduction in the risk of disease worsening or death (42%); ORR (66% vs 24%); m-PFS (not reached vs 4.11 mos.); Grade 3 AEs (48% vs. 44%)
  • Tiragolumab is a mAb designed to bind with TIGIT and works as an immune amplifier- by potentially enhancing the body’s immune response. The company is evaluating the tiragolumab across various settings in different tumor types- including lung- esophageal and cervical cancers

 ­ Ref: BusinessWire | Image: Genentech

Click here to­ read the full press release 

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