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Clinical Trial of Rituximab in Children and Adolescents With Chronic Idiopathic Thrombocytopenic Purpura (ITP)

Phase 1
Completed
Conditions
Idiopathic Thrombocytopenic Purpura (ITP)
Immune Thrombocytopenic Purpura (ITP)
Interventions
Registration Number
NCT01713738
Lead Sponsor
Neufeld, Ellis J, MD, PhD
Brief Summary

The purpose of the study is to evaluate the safety and efficacy of rituximab in children ages 18 months to 18 years, who have severe, chronic ITP. Eligible patients with either primary or secondary ITP are treated with rituximab once a week for 4 doses, and then followed for up to one year. Response is defined as having a platelet count greater than or equal to 50,000/mL on four consecutive weekly measures beginning anytime in weeks 9 - 12.

Detailed Description

The purpose of this open label, phase I/II study is to evaluate the safety and efficacy of rituximab in children ages 18 months to 18 years, who have severe, chronic ITP. Eligible patients with either primary or secondary ITP are treated with rituximab once a week for 4 doses, and then followed for up to one year. The primary and secondary objectives for safety and efficacy are as follows:

Primary

1. Efficacy: To evaluate the effectiveness of rituximab in severe or refractory pediatric ITP, with response defined as follows: platelet count greater than or equal to 50,000/mL on four consecutive weekly measures beginning anytime in weeks 9 - 12 (day 57 - day 84), with the first and fourth measure being spaced at least 22 days apart (i.e., once established during the 9 - 12 week timeframe, the response would be defined as beginning at the first one of these measures). All measurements must be independent of supportive care, as follows: 1) no IVIG (intravenous immunoglobulin) administration within 7 days of the first measure or at any time between measures, 2) no initiation of a 4-day corticosteroid "pulse" within 7 days of the first measure or at any time between measures, 3) no RHo (D) immunoglobulin (WinRHo-SDFTM ) administration within 7 days of the first measure or at any time between measures, and 4) no platelet transfusions administered within 7 days of the first measure or at any time between measures.

2. Safety: To obtain further safety information on rituximab in this clinical setting using Genentech standard safety monitoring and SAE reporting. In addition, the frequency of hypogammaglobulinemia will be assessed as the incidence of IgG levels \<1/2 the lower limit of normal for age.

Secondary

1. To evaluate the one-year clinical course of severe or refractory ITP patients treated with a single course of rituximab. What fraction of responsive patients maintains this response?

2. To assess the need for salvage therapy (supportive care) in this severely affected group of patients during the clinical trial.

3. To evaluate the rate of "early response," defined as: platelets greater than or equal to 50,000/mL at least one week off rescue therapy, BEFORE day 57, and continuing for four consecutive weeks.

4. To follow the trend of bleeding scores from onset of therapy through the duration of the trial.

5. To assess the incidence of hypogammaglobulinemia requiring intervention (IgG level \<1/2 of lower limit of normal for age) in this setting. IVIG 400 mg/kg monthly will be used to treat hypogammaglobulinemia.

6. To describe the health-related quality of life (HRQL) of children with severe or refractory ITP, based on parent report and to assess the impact on the family, using standardized questionnaires. This is a pilot-scale objective.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
36
Inclusion Criteria

severe, chronic ITP, including refractory; at least 6 months from diagnosis for refractory; at least 12 months from diagnosis for severe; platelet counts <10,000/mm3 twice in past 3 months without bleeding; platelet counts <20,000/mm3 twice in past 3 months with bleeding

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Exclusion Criteria

ever had B or T cell neoplasm; HIV/AIDS; allergy to murine antibodies; treatment with investigational immunosuppressive strategies within past 3 months -

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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
rituximabrituximab-
Primary Outcome Measures
NameTimeMethod
platelet levels9 - 12 weeks after 1st dose of rituximab
hypogammaglobulinemiaover one year
Secondary Outcome Measures
NameTimeMethod
fraction of responsive patients maintaining response over 1 yearweek 52
assessment of need for salvage therapyfirst 12 weeks of trial
rate of early response before day 57before day 57, and 4 additional weeks
trend of bleeding scores throughout trialover one year
description of health-related quality of lifeover one year

Trial Locations

Locations (9)

Stanford University School of Medicine

🇺🇸

Palo Alto, California, United States

University of California, San Francisco

🇺🇸

San Francisco, California, United States

Emory University School of Medicine

🇺🇸

Atlanta, Georgia, United States

Van Eslander Cancer Center, St. John Hospital

🇺🇸

Detroit, Michigan, United States

Southwestern Medical Center at Dallas

🇺🇸

Dallas, Texas, United States

Weill Medical College at Cornell University

🇺🇸

New York, New York, United States

Baylor College of Medicine

🇺🇸

Houston, Texas, United States

Children's Hospital Boston

🇺🇸

Boston, Massachusetts, United States

UCLA, Mattel Children's Hospital

🇺🇸

Los Angeles, California, United States

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