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Clinical trialNCT01713738CompletedPhase 1/PHASE2Interventional

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

SponsorNeufeld, Ellis J, MD, PhDEnrollment36Idiopathic Thrombocytopenic Purpura (ITP)Immune Thrombocytopenic Purpura (ITP)
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

9 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Ucla, Mattel Children'S Hospital

    Los Angeles, California, United States

  • 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

  • Children'S Hospital Boston

    Boston, Massachusetts, United States

  • Van Eslander Cancer Center, St. John Hospital

    Detroit, Michigan, United States

  • Weill Medical College at Cornell University

    New York, New York, United States

  • Southwestern Medical Center at Dallas

    Dallas, Texas, United States

  • Baylor College of Medicine

    Houston, Texas, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 May 2003
Primary completion
31 Dec 2005
Completion
31 Dec 2005
Last update posted
9 Nov 2012
Registered enrollment
36
Registry id
NCT01713738

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.