Apatinib Combined with Albumin-Bound Paclitaxel for Treatment of Advanced Triple Negative Breast Cancer
- Sponsor
- Fujian Cancer Hospital
- Study ID
- NCT05019690
- Phase
- PHASE1/PHASE2
- Status
- Recruiting
Conditions
- Advanced Triple Negative Breast Cancer
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Apatinib Mesylate — DRUGSubjects receive Apatinib orally, Dosage form: tablet, Strength: 250 mg/tablet,QD,Q3W
- Albumin-Bound Paclitaxel — DRUGSubjects receive Albumin-Bound Paclitaxel,ivgtt, Strength: 125 mg/m\^2,d1、7、15,Q3W
Study Details
This study is a single-arm,exploratory clinical study, to evaluate the effectiveness and safety of apatinib mesylate combined with albumin-bound paclitaxel for second-line treatment of advanced triple negative breast cancer.
Key Dates
- Start date
- Oct 1, 2021
- Status verified
- Sep 2024
- Primary completion
- Dec 1, 2024
- Completion
- Jun 1, 2025
Study Design
- Enrollment
- 29 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Apatinib Combined With Albumin-Bound PaclitaxelParticipants will receive apatinib combined with albumin-bound paclitaxel until predefined study end, disease progression, unacceptable toxicity, withdrawal of consent or death, whichever occurs first.
Primary Outcome Measure
Progression-Free Survival(PFS) [ Time Frame: From enrollment to 12 month ]
Central Contacts
- weiwei Huang13763893896
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