Viewing Study NCT01204177



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Last Modification Date: 2024-10-26 @ 10:25 AM
Study NCT ID: NCT01204177
Status: COMPLETED
Last Update Posted: 2013-09-06
First Post: 2010-09-16

Brief Title: Assessing BAY86-9766 Plus Sorafenib for the Treatment of Liver Cancer
Sponsor: Bayer
Organization: Bayer

Study Overview

Official Title: A Phase II Trial of BAY86-9766 Plus Sorafenib as First Line Systemic Treatment for Hepatocellular Carcinoma HCC
Status: COMPLETED
Status Verified Date: 2013-09
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: BASIL
Brief Summary: This study investigates the safety and efficacy of the combination therapy with BAY86-9766 and sorafenib in patients with liver cancer Safety will be determined by laboratory and other evaluations Efficacy of the combination BAY86-9766 and sorafenib will be determined by disease control rate overall survival time to progression response rate and duration of response
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