Clinical trial

Efficacy and Safety Study of OSI-211 (Liposomal Lurtotecan) to Treat Recurrent…

NCT00046787 · Astellas Pharma Inc, Industry · Completed

Key facts

NCT number NCT00046787
Title Efficacy and Safety Study of OSI-211 (Liposomal Lurtotecan) to Treat Recurrent Small Cell Lung Cancer
Official title Phase II Study to Determine the Efficacy of OSI-211 (Liposomal Lurtotecan) Given on Days 1, 2 & 3 Every 3 Weeks in Patients With Recurrent Small Cell Lung Cancer
Lead sponsor Astellas Pharma Inc, Industry
Collaborators OSI Pharmaceuticals Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions SCLC, Carcinoma, Small Cell
Intervention type Drug
Interventions OSI-211 (Liposomal Lurtotecan)
Enrollment 47
Start date Sep 1, 2002
Completion Feb 1, 2003
First posted Oct 4, 2002
Last update posted Oct 20, 2011
Countries United Kingdom, United States

At a glance

  • 10–99 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.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

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

Browse all ClinicalTrials.gov studies