RecruitingNCT07035886

A Study to Monitor the Fruzaqla Treatment of Adults With Metastatic Colorectal Cancer (mCRC) in South Korea

Post-Marketing Surveillance (Usage Results Study) of Fruzaqla Capsule (Fruquintinib) for the Approved Indications in South Korea


Sponsor

Takeda

Enrollment

600 participants

Start Date

Sep 29, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • Age greater than or equal to (\>=)18 years.
  • Participants who are initiate treatment or will be treated with Fruzaqla according to the approved label of South Korea.
  • Participant voluntarily consent to participate in the study.

Exclusion Criteria3

  • Participants for whom Fruzaqla is contraindicated or those with risks that should avoid starting Fruzaqla, as per the product label.
  • Participants actively participating in other interventional clinical trial(s) on mCRC treatments.
  • Pregnant or breastfeeding women.

Interventions

OTHERNo intervention

As this is an observational study, no intervention will be administered.


Locations(1)

Yonsei University Hospital

Seoul, South Korea

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NCT07035886


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