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Weekly Docetaxel and Fixed-Dose Rate Gemcitabine Combination Chemotherapy

Sarcoma Clinical Trial

Official title:
Phaseâ…¡ Study of Weekly Docetaxel and Fixed-Dose Rate Gemcitabine in Patient With Previously Treated Advanced Soft Tissue and Bone Sarcoma Prospective, Open Label, Multi-Institutional

Clinical Trial Summary

To determine the activity of weekly Docetaxel and Gemcitabine in patients with advanced soft tissue sarcoma previously treated with anthracycline and/or ifosfamide

1. Primary endpoint: response rate

2. Secondary endpoint: progress-free survival, overall survival, safety

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00807261
Study type Interventional
Source Asan Medical Center
Contact
Status Enrolling by invitation
Phase Phase 2
Start date September 2008
Completion date September 2010
View Details
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