Participants with select solid tumors will receive a recommended dose of RO7502175, determined in Phase Ib Dose Escalation phase, as an IV infusion, in combination with a fixed dose of atezolizumab, as an IV infusion on Day 1 of each 21-day cycle until disease progression or unacceptable toxicity.
RO7502175 will be administered as per the schedules specified in the respective arms.
Atezolizumab will be administered as per the schedules specified in the respective arms.
Source: View full study details on ClinicalTrials.gov
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