Viewing Study NCT00086203



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Last Modification Date: 2024-10-26 @ 9:10 AM
Study NCT ID: NCT00086203
Status: COMPLETED
Last Update Posted: 2015-03-25
First Post: 2004-06-28

Brief Title: Study of Talabostat and Rituximab in Advanced Chronic Lymphocytic Leukemia CLL
Sponsor: Point Therapeutics
Organization: FDA Office of Orphan Products Development

Study Overview

Official Title: None
Status: COMPLETED
Status Verified Date: 2006-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The objective of this study is to assess the efficacy and safety of talabostat and rituximab in patients with advanced CLL who failed to respond or have progressed following a prior response to a fludarabine regimen
Detailed Description: Completion date provided represents the completion date of the grant per OOPD records

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
FD-R-003021-01 None None None