204
Participants
Start Date
November 15, 2021
Primary Completion Date
January 20, 2025
Study Completion Date
January 20, 2025
NIS793
Investigational drug NIS793 will be administered intravenously (IV) at the dose and schedule determined in the safety run-in part.
Bevacizumab
Bevacizumab will be administered IV
Modified FOLFOX6
5-fluorouracil \[continuous infusion\], leucovorin \[administered IV\] (or levoleucovorin \[administered IV\]), and oxaliplatin \[administered IV\]
FOLFIRI
5-fluorouracil \[continuous infusion\], leucovorin \[administered IV\] (or levoleucovorin \[administered IV\]), and irinotecan \[administered IV\]
Tislelizumab
Investigational drug tislelizumab will be administered intravenously (IV).
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Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY