153
Participants
Start Date
December 17, 2021
Primary Completion Date
December 31, 2029
Study Completion Date
December 31, 2032
Panitumumab 20 milligram/ML
Participants receive Panitumumab at 6mg/ kg intravenously (IV) on Day 1 and 15 of each 28-day cycle. Treatment is continued until occurrence of progression according to RECIST 1.1 criteria as evaluated by the investigator or unacceptable toxicity.
Bevacizumab
Participants receive bevacizumab at 5 mg/ kg intravenously (IV) on Day 1 and 15 of each 28-day cycle. Treatment is continued until occurrence of progression according to RECIST 1.1 criteria as evaluated by the investigator or unacceptable toxicity.
Trifluridine/Tipiracil Hydrochloride
Participants receive Trifluridine/tipiracil at 35 mg/m² BSA, twice daily, orally on days 1-5 and 8-12
RECRUITING
Charité - Universitätsmedizin Berlin, Berlin
Dominik Paul Modest
OTHER