Viewing Study NCT00047801



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Last Modification Date: 2024-10-26 @ 9:08 AM
Study NCT ID: NCT00047801
Status: COMPLETED
Last Update Posted: 2011-07-25
First Post: 2002-10-18

Brief Title: Phase 1-2a Dose-Ranging Study of TLK286 in Combination With Docetaxel in Platinum-Resistant Non-Small Cell Lung Cancer
Sponsor: Telik
Organization: Telik

Study Overview

Official Title: Phase 1-2a Dose-Ranging Study of TLK286 in Combination With Docetaxel Taxotere in Platinum-Resistant Non-Small Cell Lung Cancer
Status: COMPLETED
Status Verified Date: 2011-06
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 purpose of this study is to determine the effectiveness and safety of TLK286 given intravenously once every three weeks in combination with docetaxel Taxotere in the treatment of patients with non-small cell lung cancer that is resistant to platinum-based 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