Immune Thrombocytopenia (ITP) Clinical Trial
Official title:
Rituximab as Second Line Treatment for ITP; A Multicenter, Randomized, Double Blind, Placebo-controlled, Phase III Study. "The RITP Study"
Immune thrombocytopenic purpura (ITP) is an autoimmune disorder characterized
thrombocytopenia.
Splenectomy is the standard treatment for patients who fails the first-line treatment:
corticosteroid. Rituximab, has recently emerged as a promising treatment for ITP. The aim of
the study is to determine whether early treatment with Rituximab can result in durable
remissions, and consequently, lead to the avoidance of splenectomy in a significant number
of patients.
ITP is an autoimmune disorder characterized by formation of autoantibodies against platelet
antigens leading to premature platelet destruction and persistent thrombocytopenia often
resulting in bleeding.
The goal of treatment is to raise the platelet count to a hemostatically safe level.
Treatment with corticosteroids rarely results in durable responses, and most of the patients
will ultimately require a second-line treatment. Splenectomy results in a high rate of
sustained remissions. However, the procedure is invasive and is associated with considerable
short and long term morbidity and mortality. Rituximab, a chimeric anti-CD20 antibody with a
B-cell depleting effect, has recently emerged as a promising treatment for ITP.
The study aims to determine whether early treatment with Rituximab can result in durable
remissions, and consequently, avoidance of splenectomy in a clinical significant number of
patients.
The main objective of this study is to assess the rate of treatment failure (splenectomy or
meeting criteria for splenectomy after week 12) at 1.5-year in a prospective, randomized,
placebo-controlled, double-blind, multi-centre
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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