5-FU
DrugIntravenous repeating dose
NCT Number: NCT01418222
This randomized, double-blind, placebo-controlled study will evaluate the efficacy and safety of FOLFOX/bevacizumab with onartuzumab (MetMAb) versus placebo as first-line treatment in patients with metastatic colorectal cancer.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Almac Clinical Technologies, San Francisco, California, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Intravenous repeating dose
Intravenous repeating dose
Intravenous repeating dose
Intravenous repeating dose
Intravenous repeating dose
Intravenous repeating dose
Time frame: up to 4 years
Time frame: up to 4 years
Time frame: up to 4 years
Time frame: up to 4 years
Time frame: up to 4 years
Genentech, Inc.
Industry
Randomized, Double-Blind, Phase II Study of FOLFOX/Bevacizumab With Onartuzumab (MetMAb) Versus Placebo as First-Line Treatment for Patients With Metastatic Colorectal Cancer
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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