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Clinical Trial Summary

The primary objective of this study is to assess the safety profile of copanlisib at the recommended dose (primary endpoint). The recommended dose of copanlisib for Japanese patients will be determined in the dose escalation/safety evaluation part.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02342665
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 1/Phase 2
Start date April 21, 2015
Completion date February 10, 2022

See also
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