TerminatedPhase 3NCT00799773

Evaluating the Effectiveness of Adding Rituximab to Standard Treatment for Thrombotic Thrombocytopenic Purpura (TTP)

Studying Congenital thrombotic thrombocytopenic purpura

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Key facts

Sponsor
Carelon Research
Principal Investigator
Susan F. Assmann, PhD
New England Research Institutes, Inc.
Intervention
Rituximab(drug)
Enrollment
3 enrolled
Eligibility
12 years · All sexes
Timeline
20092010

Study locations (23)

Collaborators

National Heart, Lung, and Blood Institute (NHLBI) · Genentech, Inc.

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT00799773 on ClinicalTrials.gov

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