Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06125080

The Efficacy and Safety of Utidelone Plus Tirelizumab and Bevacizumab for Advanced or Metastatic Triple-negative Breast Cancer (UTILIZABLE) :Single-arm, Prospective, Open Clinical Study

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
78 (estimated)
Sponsor
Huihua Xiong · Academic / Other
Sex
Female
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

This is a multicenter, open-label, single-arm clinical study designed to evaluate the safety and efficacy of Utidelone plus Tirelizumab and Bevacizumab for advanced or metastatic triple-negative breast cancer (TNBC).

Conditions

Interventions

TypeNameDescription
DRUGUtideloneUtidelone (30 mg/m2, days 1-5, every 3 weeks)
DRUGTirelizumabTirelizumab(200mg, day1, every 3 weeks)
DRUGBevacizumabBevacizumab(7.5mg/kg, day1, every 3 weeks)

Timeline

Start date
2023-10-30
Primary completion
2025-10-30
Completion
2026-10-30
First posted
2023-11-09
Last updated
2023-11-09

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06125080. Inclusion in this directory is not an endorsement.

The Efficacy and Safety of Utidelone Plus Tirelizumab and Bevacizumab for Advanced or Metastatic Triple-negative Breast (NCT06125080) · Clinical Trials Directory