Trials / Unknown
UnknownNCT02947061
S1 Plus Docetaxel Versus Capecitabine Plus Docetaxel First-line Treatment in Patients With Advanced Breast Cancer
S1 Plus Docetaxel Versus Capecitabine Plus Docetaxel First-line Treatment in Patients With Advanced Breast Cancer: a Phase 2, Prospective,Multicenter, Randomised Study
- Status
- Unknown
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 300 (estimated)
- Sponsor
- Chinese Academy of Medical Sciences · Academic / Other
- Sex
- Female
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
To compare the progression free survival(PFS) and safety of TS-S vs. TX-X in Patients With Advanced Breast Cancer first-line treatment
Detailed description
To compare progression free survival (PFS) of the S-1 combined with docetaxel followed by maintenance treatment with S-1 and capecitabine combined with docetaxel followed by maintenance therapy with capecitabine in patients with advanced breast cancer first-line treatment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | S1 plus Docetaxel | S1 80mg to 120 mg per day on Days 1-14, every 21 days; Docetaxel 75mg/m2 on Day 1 |
| DRUG | Capecitabine plus Docetaxel | Capecitabine 1,000 mg/m2 per day on Days 1-14, every 21 days; Docetaxel 75mg/m2 on Day 1 |
Timeline
- Start date
- 2015-04-01
- Primary completion
- 2017-04-01
- Completion
- 2019-04-01
- First posted
- 2016-10-27
- Last updated
- 2016-10-31
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT02947061. Inclusion in this directory is not an endorsement.