Viewing Study NCT00434642



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Last Modification Date: 2024-10-26 @ 9:30 AM
Study NCT ID: NCT00434642
Status: COMPLETED
Last Update Posted: 2017-08-09
First Post: 2007-02-09

Brief Title: A Study of Carboplatin and Gemcitabine Plus Bevacizumab in Patients With Ovary Peritoneal or Fallopian Tube Carcinoma
Sponsor: Genentech Inc
Organization: Genentech Inc

Study Overview

Official Title: A Phase III Multicenter Randomized Blinded Placebo-controlled Trial of Carboplatin and Gemcitabine Plus Bevacizumab in Patients With Platinum-sensitive Recurrent Ovary Primary Peritoneal or Fallopian Tube Carcinoma
Status: COMPLETED
Status Verified Date: 2017-07
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: OCEANS
Brief Summary: This is a placebo-controlled randomized multicenter Phase III study that will evaluate the safety and efficacy of bevacizumab administered in combination with carboplatin with gemcitabine in women with platinum-sensitive recurrent epithelial ovarian primary peritoneal or fallopian tube carcinoma
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