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
| Type | Name | Description |
|---|---|---|
| DRUG | Utidelone | Utidelone (30 mg/m2, days 1-5, every 3 weeks) |
| DRUG | Tirelizumab | Tirelizumab(200mg, day1, every 3 weeks) |
| DRUG | Bevacizumab | Bevacizumab(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.