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.
Protocol Amendment History
3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2025-06-17; most recent amendment 2026-02-26.
Status change: Not Yet Recruiting → Recruiting2025-11-25