Viewing Study NCT00960349



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Last Modification Date: 2024-10-26 @ 10:09 AM
Study NCT ID: NCT00960349
Status: COMPLETED
Last Update Posted: 2011-06-14
First Post: 2009-08-11

Brief Title: Study of Cediranib Plus Cisplatin Plus CapecitabineS-1 in Japanese Gastric Cancer Patients
Sponsor: AstraZeneca
Organization: AstraZeneca

Study Overview

Official Title: A Phase I Open-label Non-randomized Study to Assess the Safety and Tolerability of Cediranib AZD2171 in Combination With Cisplatin Plus a Fluoropyrimidine Capecitabine or S-1 in Japanese Patients With Previously Untreated Locally Advanced or Metastatic Unresectable Gastric Cancer
Status: COMPLETED
Status Verified Date: 2011-06
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 primary objective of the study is to assess the safety and tolerability of cediranib in combination with Cisplatin plus a Fluoropyrimidine Capecitabine or S-1 in Japanese patients with previously untreated locally advanced or metastatic unresectable gastric cancer GC
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