Inosine Reverse Chemo Resistance in Triple Negative Breast Cancer
- Sponsor
- Fudan University
- Study ID
- NCT06355024
- Phase
- PHASE2
- Status
- Completed
Conditions
- Triple-negative Breast Cancer
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - 70 Years
- Healthy Volunteers
- Not accepted
Interventions
- Inosine — DRUGoral inosine 200mg tid
- Taxane/Anthracycline/Eribulin Mesylate/Vinorelbine/Capecitabine/Carboplatin/UTD1/platinum — DRUGTaxane/Anthracycline/Eribulin Mesylate/Vinorelbine/Capecitabine/Carboplatin/UTD1/platinum
Study Details
This is a Phase II, open-label, single-arm study evaluating the efficacy and safety of combined treatment of Inosine with chemotherapy in mTNBC (triple negative breast cancer) patients who progressed during previous chemotherapy.
Key Dates
- Start date
- May 11, 2024
- Status verified
- Jul 2025
- Primary completion
- Jan 1, 2025
- Completion
- Jan 1, 2025
Study Design
- Enrollment
- 10 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Inosineoral inosine arm
Primary Outcome Measure
Objective Response Rate (ORR) [ Time Frame: Baseline until disease progression or loss of clinical benefit, assessed up to 6 months ]
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