Condition: Colorectal Cancer · Sponsor: Takeda
The purpose of this study is to estimate the proportion of all adverse events (AEs) including serious adverse events (SAEs) occurring with the use of fruquintinib among adult participants who have been administered fruquintinib as per the approved indications.
This description comes directly from the study's public registry record.
Takeda Contact · +1-877-825-3327 · medinfoUS@takeda.com
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| Yonsei University Hospital | Seoul, South Korea | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07035886