Clinical Study of Second-line Treatment in Advanced Colorectal Cancer With Chemotherapy With Bevacizumab or Cetuximab

NCT06540326 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2025-12-22

No results posted yet for this study

Summary

Guidelines recommend FOLFIRI in combination with bevacizumab or cetuximab as a treatment option for advanced second-line colorectal cancer, and this study explores the efficacy and safety of a clinical study of liposomal irinotecan (II), fluorouracil, in combination with bevacizumab or cetuximab for the second-line treatment of patients with advanced colorectal cancer.

Conditions

  • Colorectal Cancer Metastatic

Interventions

DRUG

irinotecan liposome (II)

irinotecan liposome (II) is a powerful chemotherapeutic agents, in the combination with fluorouracil,and bevacizumab or cetuximab

DRUG

fluorouracil

fluorouracil is a powerful chemotherapeutic agents, in the combination with irinotecan liposome (II),and bevacizumab or cetuximab

DRUG

cetuximab

cetuximab is a powerful targeted agents, in the combination with irinotecan liposome (II),and fluorouracil

DRUG

bevacizumab

bevacizumab is a powerful targeted agents, in the combination with irinotecan liposome (II),and fluorouracil

DRUG

Capecitabine

Capecitabine is a powerful chemotherapeutic agent, in the combination with bevacizumab or cetuximab

Sponsors & Collaborators

  • Second Affiliated Hospital, School of Medicine, Zhejiang University

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-11-12
Primary Completion
2026-04-15
Completion
2027-10-31

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06540326 on ClinicalTrials.gov