Rituximab as Second Line Treatment for ITP
- Sponsor
- Ostfold Hospital Trust
- Study ID
- NCT00344149
- Phase
- PHASE3
- Status
- Completed
Conditions
- Immune Thrombocytopenia (ITP)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Rituximab (Mabthera) — DRUGI.V infusion of Rituximab 375 mg/m2 per week for 4 weeks
Study Details
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.
Key Dates
- Start date
- Jun 30, 2006
- Status verified
- Mar 2014
- Primary completion
- Mar 31, 2014
- Completion
- Mar 31, 2014
Study Design
- Enrollment
- 112 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: RituximabI.V infusion of Rituximab 375 mg/m2 per week for 4 weeks
- Placebo Comparator: PlaceboI.V infusion of NaCl 0.9%
Primary Outcome Measure
The primary endpoint is treatment failure as defined by a composite end point of Splenectomy performed at any time after randomization or Meeting the predefined Criteria for Splenectomy at or after week 12 that is if splenectomy is not performed. [ Time Frame: 1.5 years ]
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