Viewing Study NCT00473616



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Last Modification Date: 2024-10-26 @ 9:32 AM
Study NCT ID: NCT00473616
Status: TERMINATED
Last Update Posted: 2011-02-11
First Post: 2007-05-14

Brief Title: Phase I Single Ascending DoseMultiple Ascending Dose in Patients Treated With AZD7762 and Irinotecan
Sponsor: AstraZeneca
Organization: AstraZeneca

Study Overview

Official Title: A Phase I Open-label Multi-center Dose-escalation and Safety Expansion Study to Assess Safety Tolerability and Pharmacokinectics of AZD7762 Administered as a Single Intravenous Agent and in Combination With Weekly Standard Dose of Irinotecan in Patients With Advanced Solid Malignancies
Status: TERMINATED
Status Verified Date: 2011-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Termination of the study was made after a full review of program data and assessment of the current risk-benefit profile
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is an open-label multi-center dose-escalation and safety expansion Phase I study to evaluate the safety tolerability and pharmacokinectics and to investigate biomarker changes of AZD7762 administered as a single intravenous unit and in combination with irinotecan The study is sponsored by AstraZeneca
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