Viewing Study NCT00193492


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Study NCT ID: NCT00193492
Status: COMPLETED
Last Update Posted: 2015-01-05
First Post: 2005-08-22
Is NOT Gene Therapy: True
Has Adverse Events: True

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

Study Overview

Official Title: Rituximab +/- Bevacizumab in the Treatment of Patients With Follicular Non-Hodgkin's 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-hodgkin's 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: True
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?:

Secondary ID Infos

Secondary ID Type Domain Link View
U3234s OTHER Genentech-Roche View