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Not Yet RecruitingNCT06092242

The Efficacy and Safety of TAS-102(Suyuan) Combined With Bevacizumab as First-line Therapy in Patients With Advanced Colorectal Cancer

Status
Not Yet Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
The Second Affiliated Hospital of Shandong First Medical University · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

To evaluate the efficacy and safety of TAS-102 combined with bevacizumab as first-line therapy in patients with advanced colorectal cancer who could not tolerate or did not receive combined chemotherapy

Conditions

Interventions

TypeNameDescription
DRUGTas-102(Suyuan) combined with bevacizumabTas-102: po 35 mg/m2, bid, d1-5, d8-12, Q4 wks; bevacizumab: intravenous drip 5 mg/kg, D1, D15, Q4 wks.

Timeline

Start date
2023-10-15
Primary completion
2025-10-15
Completion
2027-10-15
First posted
2023-10-23
Last updated
2023-10-23

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06092242. Inclusion in this directory is not an endorsement.

The Efficacy and Safety of TAS-102(Suyuan) Combined With Bevacizumab as First-line Therapy in Patients With Advanced Col (NCT06092242) · Clinical Trials Directory