Actively Recruiting

Age: 19Years +
All Genders
NCT07263178

A Study of Second- and Later-line Palliative Chemotherapy in Patients With Metastatic Colorectal Cancer.

Led by Boryung Pharmaceutical Co., Ltd · Updated on 2025-12-04

1000

Participants Needed

1

Research Sites

212 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to comprehensively identify the various treatment patterns of second- or subsequent-line palliative chemotherapy used in patients with metastatic colorectal cancer who have experienced failure of first-line palliative chemotherapy and to evaluate the prognosis of each treatment.

CONDITIONS

Official Title

A Study of Second- and Later-line Palliative Chemotherapy in Patients With Metastatic Colorectal Cancer.

Who Can Participate

Age: 19Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients who have signed informed consent after learning about the study's purpose and methods
  • Patients with histologically and radiologically confirmed metastatic colorectal cancer with measurable lesions
  • Patients scheduled to receive their first second-line palliative chemotherapy after failure of first-line treatment or relapse within 6 months after finishing postoperative adjuvant therapy
  • Patients who understand the study, cooperate with the process, and can participate until the study ends
Not Eligible

You will not qualify if you...

  • Female patients who are pregnant, breastfeeding, or have childbearing potential
  • Patients who have used an investigational product within 4 weeks before enrollment or plan to join another clinical trial during this study
  • Patients considered unsuitable for participation by the investigator's judgment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Samsung Medical Center

Seoul, South Korea

Actively Recruiting

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Research Team

S

Shinyoung Oh

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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