Clinical Trials Directory

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

TypeNameDescription
DRUGS1 plus DocetaxelS1 80mg to 120 mg per day on Days 1-14, every 21 days; Docetaxel 75mg/m2 on Day 1
DRUGCapecitabine plus DocetaxelCapecitabine 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.