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Clinical Trial Summary

The purpose of Phase 1b of the study is to determine the maximum tolerated dose, pharmacokinetics (PK) and pharmacodynamics (PDn) and assess the safety, tolerability and activity of oprozomib in combination with sorafenib in subjects with advanced hepatocellular carcinoma (HCC).

The purpose of Phase 2 of the study is to evaluate the efficacy of oprozomib in combination with sorafenib versus sorafenib alone and to compare the key outcome measures for subjects with advanced HCC.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02227914
Study type Interventional
Source Amgen
Contact
Status Withdrawn
Phase Phase 1/Phase 2
Start date December 2014
Completion date March 2015

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