Non-Small Cell Lung Cancer Clinical Trial
Official title:
A Phase III, Randomized, Double-Blind, Multi-Center Study of the Efficacy of Taxotere (Docetaxel) in Combination With Aptosyn (Exisulind) Versus Taxotere (Docetaxel) and Placebo in Non-Small Cell Lung Cancer (NSCLC) Patients After Failure of Prior Platinum-Based Chemotherapy
Taxotere has been approved by the FDA and is considered a standard treatment for patients
with lung cancer who have failed prior platinum-containing regimens. The main purpose of
this research study is to determine if Aptosyn, when given in combination with Taxotere,
will result in prolonged survival when compared to Taxotere alone.
This study will also help determine tumor response rates, and the safety profile of Aptosyn
in combination with Taxotere.
This study has been completed and a publication is pending.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
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