NCT06060704

Envafolimab Combined With Trifluridine/Tipiracil and Bevacizumab in the Treatment of Refractory mCRC.

A Prospective, Open, Single-center, Single-arm Study to Explore Envafolimab Combined With Trifluridine/Tipiracil and Bevacizumab in the Treatment of mCRC Patients Who Were Refractory to Second-line and Above Standard Therapy.
The First Affiliated Hospital with Nanjing Medical University·Phase 2·ClinicalTrials.gov·drugRecruiting
View on ClinicalTrials.gov
Study focus
Drug/Device/Intervention
Envafolimab
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
The First Affiliated Hospital with Nanjing Medical University
Location
Nanjing, China
Timeline & enrollment
Phase
Phase 2
Start date
Nov 01, 2023
End date
Sep 01, 2025
Enrollment
33 participants
Primary outcome

ORR(Objective response rate)

Summary

The goal of this single-arm study is to evaluate the efficacy and safety of Envafolimab
 combined with Trifluridine/Tipiracil and Bevacizumab in the treatment of metastatic
 colorectal cancer patients who are refractory or intolerant to standard therapy.

ICD-10 classifications
Malignant neoplasm of colonMalignant neoplasm: Colon, unspecifiedMalignant neoplasm: Descending colonMalignant neoplasm: Ascending colonMalignant neoplasm: Overlapping lesion of colon
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06060704
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06060704 through Pure Global AI's free database. This Phase 2 trial is sponsored by The First Affiliated Hospital with Nanjing Medical University and is currently Recruiting. The study focuses on Metastatic Colorectal Cancer. Target enrollment is 33 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.