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Phase II Trial of Thalidomide (Thalidomide Pharmion) in Patients With Advanced or Relapsed Lymphoma of the Mucosa Associated Lymphoid Tissue (MALT)
The purpose of this study is to evaluate Thalidomide for treatment of disseminated MALT Lymphoma or at relapse following helicobacter pylori (HP) - eradication or chemotherapy or radiation.
The objectives of this study are to evaluate the effectivity and the safety of thalidomide in patients with disseminated MALT lymphoma or at relapse following HP-eradication, or chemotherapy or radiation. It is a phase II prospective single arm study with a target sample size of 16 patients. Thalidomide is given orally at an initial dose of 100 mg for a maximum duration of 6 months.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Department of Internal Medicine I
Vienna, Austria
Start Date
June 1, 2006
Primary Completion Date
January 1, 2009
Completion Date
January 1, 2009
Last Updated
June 18, 2009
8
ACTUAL participants
Thalidomide, Pharmion
DRUG
Lead Sponsor
Medical University of Vienna
NCT06228963
NCT01808599
Data Source & Attribution
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