Roche announced that the European Commission (EC) has granted it marketing authorisation for Tecentriq® SC (atezolizumab) for subcutaneous injection. The new authorisation applies to all indications already approved for the previous formulation of Tecentriq® (administered by IV infusion) including various lung, liver, bladder and breast cancers.
The Committee for Medicinal Products for Human Use (CHMP) recommended the approval of Tecentriq® SC (the new formulation) on 14 November 2023.