drugset / Trial / NCT00807261

Weekly Docetaxel and Fixed-Dose Rate Gemcitabine Combination Chemotherapy

NCT00807261 ↗

Non-randomizedSingle-groupOpen-labelSupportive care

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

Timeline

Start
2008-09
Primary completion
2010-09
Completion
2010-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Docetaxel Small molecule 35 mg/m2 Intravenous
Subject Gemcitabine Small molecule 1000 mg/m2 Intravenous

Indications