Viewing Study NCT00171834



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Last Modification Date: 2024-10-26 @ 9:16 AM
Study NCT ID: NCT00171834
Status: COMPLETED
Last Update Posted: 2014-02-05
First Post: 2005-09-13

Brief Title: Dose Escalating Study of the Safety and Efficacy of Patupilone q3w in Patients With Non-small Cell Lung Cancer
Sponsor: Novartis Pharmaceuticals
Organization: Novartis

Study Overview

Official Title: An Open Label Phase III Dose Escalating Study Evaluating the Safety and Efficacy of EPO906 qw3 in Patients With Non-small Cell Lung Cancer
Status: COMPLETED
Status Verified Date: 2014-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The study objective is to evaluate the maximum tolerated dose safety and efficacy of patupilone in patients with NSCLC who have progressed after prior chemotherapy
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None