167
Participants
Start Date
May 22, 2019
Primary Completion Date
March 1, 2023
Study Completion Date
February 5, 2025
Gevokizumab
60 mg/mL concentration; administered intravenously (IV)
Bevacizumab
25 mg/mL concentration; administered IV
Modified FOLFOX6
Oxaliplatin \[5 mg/mL concentration; administered IV\], leucovorin \[10 mg/mL concentration; administered IV\] (or levoleucovorin \[10 mg/mL concentration; administered IV\]), and 5-fluorouracil \[50 mg/mL concentration; administered IV\]
FOLFIRI
Irinotecan \[20 mg/mL concentration; administered IV\], leucovorin \[10 mg/mL concentration; administered IV\] (or levoleucovorin \[10 mg/mL concentration; administered IV\]), and 5-fluorouracil \[50 mg/mL concentration; administered IV\]
Ramucirumab
10 mg/mL concentration; administered IV
Paclitaxel
6 mg/mL concentration; administered IV
Cabozantinib
60 mg tablet; administered orally
Novartis Investigative Site, Brussels
Novartis Investigative Site, Edegem
Novartis Investigative Site, Melbourne
Novartis Investigative Site, Leuven
Novartis Investigative Site, Rozzano
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Novartis Investigative Site, Madrid
Novartis Investigative Site, Madrid
Sarah Cannon Research Institute, Nashville
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WA Uni School Of Med, St Louis
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University of California LA, Los Angeles
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Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY