A Phase I, Open-Label Study of the Safety, Tolerability and Pharmacokinetics of GW572016 in Combination With Docetaxel (TAXOTERE)
Interventional
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Safety and Tolerability
GSK Clinical Trials, MD
Study Director
GlaxoSmithKline
United States: Food and Drug Administration
EGF10021
NCT00148902
April 2003
Name | Location |
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GSK Investigational Site | Germantown, Tennessee 38138 |