Viewing Study NCT00083694


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Study NCT ID: NCT00083694
Status: COMPLETED
Last Update Posted: 2010-07-02
First Post: 2004-05-27
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Thalidomide Anti-Angiogenesis Therapy of Relapsed or Refractory Leukemia
Sponsor: University of Arkansas
Organization:

Study Overview

Official Title: UARK, 98-032, Thalidomide Anti-Angiogenesis Therapy of Relapsed or Refractory Leukemia
Status: COMPLETED
Status Verified Date: 2010-07
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 purpose of this study is to evaluate the efficacy and safety of Thalidomide in patients with leukemia.
Detailed Description: Patients will take Thalidomide tablets at bedtime daily until remission. The dose will be increased gradually and modified according to side-effects. The drug will be given daily up to the time of complete remission then as long as it is beneficial.

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: