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Clinical Trial Summary

A phase IV study to characterize safety of Elunate® (Fruquintinib) in Chinese patients


Clinical Trial Description

This study is a prospective, open-label, multi-center, study design to obtain the safety information of participant after medication. The follow-up time points for each participant include first time signing the informed consent form,1 month after signing the informed consent form, 6 months after signing the informed consent form or 30 days after the last dose (whichever occurs first). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04005066
Study type Observational
Source Hutchmed
Contact
Status Completed
Phase
Start date April 20, 2019
Completion date September 27, 2022

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