Viewing Study NCT00072631



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Last Modification Date: 2024-10-26 @ 9:09 AM
Study NCT ID: NCT00072631
Status: COMPLETED
Last Update Posted: 2018-02-08
First Post: 2003-11-05

Brief Title: Erlotinib Tarceva Trademark OSI-774 in Treating Patients With Advanced Non-Small Cell Lung Cancer
Sponsor: OSI Pharmaceuticals
Organization: Astellas Pharma Inc

Study Overview

Official Title: A Phase II Open-label Intra-patient Dose-escalation Study of Erlotinib in Patients With Advanced Non-small Cell Lung Cancer Who Have Failed Prior Chemotherapy
Status: COMPLETED
Status Verified Date: 2015-06
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 if erlotinib will improve disease at doses that produce its characteristic rash in patients with advanced Non-Small Cell Lung Cancer
Detailed Description: Only patients with 0 to 1 performance status on the ECOG scale are eligible

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
Secondary IDs
Secondary ID Type Domain Link
Dose to Rash None None None