Clinical trial

A Phase III Study of the Efficacy of Taxotere/Aptosyn Versus Taxotere/Placebo in…

NCT00085826 · Astellas Pharma Inc, Industry · Completed

Key facts

NCT number NCT00085826
Title A Phase III Study of the Efficacy of Taxotere/Aptosyn Versus Taxotere/Placebo in Non-Small Cell Lung Cancer Patients
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
Lead sponsor Astellas Pharma Inc, Industry
Collaborators OSI Pharmaceuticals Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Non-Small Cell Lung Cancer
Intervention type Drug
Interventions Exisulind
Enrollment 600
Start date Apr 1, 2001
Completion Dec 1, 2004
First posted Jun 17, 2004
Last update posted Oct 20, 2011
Countries United States

At a glance

  • 100–999 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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