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Clinical Trial Summary

The objective of this Post Marketing Surveillance (PMS) is to collect and describe safety and effectiveness profile of Cabometyxâ„¢ in real clinical practice setting, according to the approved labelling after the approval of marketing authorization.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03776123
Study type Observational
Source Ipsen
Contact
Status Completed
Phase
Start date May 15, 2019
Completion date March 26, 2024

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