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Clinical Trial Summary

Phase I study of RO7119929 given orally to participants with unresectable advanced or metastatic primary liver cancers and other solid tumors with predominant liver involvement. The primary objective of the study is to explore the safety and to determine the maximum tolerated dose (MTD) and/or optimal biologic dose (OBD) of RO7119929 as single agent.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04338685
Study type Interventional
Source Hoffmann-La Roche
Contact
Status Completed
Phase Phase 1
Start date July 16, 2020
Completion date January 9, 2023

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