Viewing Study NCT00193492



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Last Modification Date: 2024-10-26 @ 9:17 AM
Study NCT ID: NCT00193492
Status: COMPLETED
Last Update Posted: 2015-01-05
First Post: 2005-08-22

Brief Title: A Study of Rituximab and Bevacizumab in Patients With Follicular Non-Hodgkins Lymphoma
Sponsor: SCRI Development Innovations LLC
Organization: SCRI Development Innovations LLC

Study Overview

Official Title: Rituximab - Bevacizumab in the Treatment of Patients With Follicular Non-Hodgkins Lymphoma A Randomized Phase II Trial
Status: COMPLETED
Status Verified Date: 2014-12
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: The purpose of this study is to assess the feasibility efficacy and safety of adding bevacizumab to rituximab compared to rituximab alone in patients with previously treated follicular non-hodgkins lymphoma NHL whose disease has progressed following at least one previous chemotherapy regimen and not more than 2 previous chemotherapy regimens
Detailed Description: Upon determination of eligibility patients will randomly be assigned to one of two treatment arms

Rituximab
Rituximab bevacizumab

For every 2 patients randomized 1 will receive treatment number 1 rituximab and 1 patient will receive treatment number 2 rituximab bevacizumab This is not a blinded study so both the patient and doctor will know which treatment has been assigned

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
Secondary IDs
Secondary ID Type Domain Link
U3234s OTHER Genentech-Roche None