Viewing Study NCT00413686



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Last Modification Date: 2024-10-26 @ 9:29 AM
Study NCT ID: NCT00413686
Status: COMPLETED
Last Update Posted: 2010-12-06
First Post: 2006-12-19

Brief Title: Study to Assess Safety of AZD7762 Administered Alone and in Combination With Gemcitabine in Patients With Advanced Solid Malignancies
Sponsor: AstraZeneca
Organization: AstraZeneca

Study Overview

Official Title: A Phase I Open Label Multi Center Dose Escalation Study to Assess Safety Tolerability and Pharmacokinetics of AZD7762 Administered as a Single Intravenous Agent and in Combination With Weekly Standard Dose Gemcitabine in Patients With Advanced Solid Malignancies
Status: COMPLETED
Status Verified Date: 2010-12
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: This is an open-label multi-center dose-escalation Phase I study to evaluate the safety tolerability and pharmacokinetics and to investigate biomarker changes of AZD7762 administered as a single intravenous unit and in combination with gemcitabine 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