A Randomized, Phase II Clinical Study of Second-line Standard Treatment Sequential TAS-102 and Bevacizumab Combined With Local Treatment in Advanced Colorectal Cancer

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This study is a randomized, controlled, open-label, phase II clinical study. This study is designed to evaluate the efficacy and safety of second-line standard treatment sequential TAS-102 and bevacizumab combined with local treatment versus continuous treatment of standard second-line therapy in advanced colorectal cancer.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Unresectable colorectal adenocarcinoma confirmed by histopathology or cytology;

• Patients who have failed first-line standard therapy and are intended to receive second-line standard therapy;

• At least one measurable lesion according to RECIST 1.1 criteria;

• ECOG Performance Status 0-1;

• Estimated life expectancy ≥3months;

• Adequate major organ function;

• Subjects voluntarily participate in this study, sign the informed consent form, and have good compliance.

Locations
Other Locations
China
Fudan University Shanghai Cancer Center
RECRUITING
Shanghai
Contact Information
Primary
Wenhua Li, Ph.D
whliiris@hotmail.com
8618017317210
Backup
Wenhua Li, Ph.D
whliiris@hotmail.com
86 18017317210
Time Frame
Start Date: 2025-02-28
Estimated Completion Date: 2027-04-30
Participants
Target number of participants: 119
Treatments
Experimental: Second-line standard therapy sequential TAS-102 and bevacizumab group
Second-line induce therapy followed by TAS-102+bevacizumab maintainance therapy combined with local treatment
Active_comparator: Continuous therapy of Standard Treatment Group
Continuous therapy of standard treatment regimen
Related Therapeutic Areas
Sponsors
Leads: Fudan University

This content was sourced from clinicaltrials.gov