Viewing Study NCT00471367



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Last Modification Date: 2024-10-26 @ 9:32 AM
Study NCT ID: NCT00471367
Status: TERMINATED
Last Update Posted: 2009-09-24
First Post: 2007-05-07

Brief Title: Phase I Open-label Dose-escalation Safety and PK Study of AZD4877
Sponsor: AstraZeneca
Organization: AstraZeneca

Study Overview

Official Title: A Phase I Open-Label Multi-Center Dose-Escalation Study to Assess the Safety Tolerability and Pharmacokinetics of AZD4877 Administered Twice a Week in Adult Patients With Advanced Solid Malignancies Including Lymphoma
Status: TERMINATED
Status Verified Date: 2009-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Part B of the study was terminated early due to a lack of enrollment
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study has two parts A and B The primary purpose of Part A is to find the maximum tolerated dose is for an experimental drug called AZD4877 based on the side effects experienced by patients that receive AZD4877 on a twice a week basis For Part B an additional 20 patients will be treated at the maximum dose identified in Part A AZD4877 is an Eg5 or Kinesin Spindle Protein inhibitor that interferes with tumor cell division leading to tumor growth
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