Viewing Study NCT00249301



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Last Modification Date: 2024-10-26 @ 9:20 AM
Study NCT ID: NCT00249301
Status: TERMINATED
Last Update Posted: 2008-04-01
First Post: 2005-11-04

Brief Title: A Study of MLN8054 in Patients With Advanced Solid Tumors
Sponsor: Millennium Pharmaceuticals Inc
Organization: Millennium Pharmaceuticals Inc

Study Overview

Official Title: An Open-Label Dose Escalation Phase 1 Study of MLN8054 a Novel Aurora A Kinase Inhibitor in Patients With Advanced Solid Tumors
Status: TERMINATED
Status Verified Date: 2008-03
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 1 The side effects or toxicities of MLN80542 The highest dose where side effects or toxicities are not too severe 3 How MLN8054 is absorbed into the general blood circulation and eliminated from the body and 4 The levels of MLN8054 in the blood that are needed to inhibit Aurora A kinase
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