New FDA approval for Genentech’s Tecentriq

18 May 2026

On Friday, the US Food and Drug Administration (FDA) approved Tecentriq (atezolizumab) and Tecentriq Hybreza (atezolizumab and hyaluronidase-tqjs), Swiss pharma giant Roche’s (ROG: SIX) subsidiary Genentech announced.

Atezolizumab is now authorized as an adjuvant treatment for adult patients with muscle-invasive bladder cancer (MIBC) who have circulating tumor DNA molecular residual disease (ctDNA MRD) after cystectomy, as identified by Natera’s Signatera CDx personalized MRD assay.

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