Start Date
September 30, 2024
Primary Completion Date
February 1, 2028
Study Completion Date
February 1, 2028
RO7617991
RO7617991 will be administered by intravenous (IV) infusion. Treatment will continue until unacceptable toxicity or loss of clinical benefit as determined by the investigator.
Tocilizumab
Tocilizumab 8 mg/kg IV will be administered to patients when necessary to treat potential cytokine release syndrome (CRS), as described in the protocol.
Lead Sponsor
Genentech, Inc.
INDUSTRY