The Efficacy of Dexamethasone Versus Dexamethasone Combined With Rituximab in Patients With Newly Diagnosed Idiopathic Thrombocytopenic Purpura (ITP)

Sponsor
Copenhagen University Hospital at Herlev
Study ID
NCT00909077
Phase
PHASE3
Status
Completed

Conditions

  • Idiopathic Thrombocytopenic Purpura

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Dexamethasone — DRUG
    Dexamethasone tablets: 40 mg/day for four days
  • Dexamethasone and Rituximab — DRUG
    Dexamethasone tablets: 40 mgs/day for four days Rituximab iv 375 mg/m\^2 weekly, a total of four times. Administered on day 2 (i.e. the patient has been treated with Dexamethasone for one day)

Study Details

In this study we want to investigate if combination therapy with rituximab (R) + dexamethasone (DXM) is superior to monotherapy with DXM in patients with newly diagnosed idiopathic thrombocytopenic purpura (ITP). Before treatment molecular studies - gene expression profiling - are performed to characterize at the molecular level those patients responding adequately to the treatment as compared to those obtaining a minor or no responses. The hypothesis is that combination therapy is superior to monotherapy as defined above. Using gene expression studies up-front the hypothesis is that this method may be able to predict the response to treatment.

Key Dates

Start date
Aug 31, 2004
Status verified
Sep 2019
Primary completion
Jun 1, 2012
Completion
Aug 1, 2017

Study Design

Enrollment
155 participants (actual)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Active Comparator: 1
    Combination therapy with Dexamethasone and Rituximab
  • Active Comparator: 2
    Dexamethasone as monotherapy

Primary Outcome Measure

Number of patients with sustained partial response after 6 months [ Time Frame: 6 months ]