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

Phase 3

Terminated

• Conditions: Thrombotic Thrombocytopenic Purpura
• Interventions: Drug: Rituximab; Procedure: Plasma exchange; Drug: Corticosteroids

• Registration Number: NCT00799773
• Lead Sponsor: Carelon Research

Brief Summary

Thrombotic thrombocytopenic purpura (TTP) is a rare disorder that causes blood clots to form in blood vessels. The main treatment for TTP is plasma exchange, in which affected patients receive transfusions of plasma, the liquid part of blood, from healthy donors. This study will examine the effectiveness of an antibody, rituximab, in combination with plasma exchange, at improving the immune response in people with TTP and decreasing the recurrence of TTP.

Detailed Description

TTP is a disorder that causes blood clots to form in the small blood vessels throughout the body. If the clots in fact block the blood vessels, blood flow is restricted to various organs, including the brain, kidneys, and heart. This can lead to neurological problems, stroke, abnormal kidney function, and heart problems. Because a large number of platelets are used in the blood clotting process, people with TTP have a reduced number of platelets circulating in their blood. They also have fewer red blood cells circulating in their blood because the red blood cells break down prematurely as blood squeezes past a blood clot.

The primary treatment for TTP is plasmapheresis, also called plasma exchange, which is a procedure that circulates a person's blood through a machine that first removes the damaged plasma and then adds healthy donor plasma into the blood. Next, patients receive a blood transfusion with the new blood. Corticosteroids, a type of medication that reduces the amount of antibodies a person's body makes, are also commonly used in conjunction with plasma exchange to treat TTP. Plasma exchange is usually effective, with platelet and red blood cell counts returning to normal after the procedure is complete. However, some people do experience a relapse of TTP and will require repeat plasma exchanges. Rituximab, an antibody currently used to treat lymphoma and rheumatoid arthritis, may improve immune system response and decrease the number of days needed to undergo the plasma exchange procedure. The purpose of this study is to evaluate the effectiveness of rituximab in combination with plasma exchange at improving an early treatment response in people with TTP and decreasing the likelihood of a relapse of TTP.

This 3-year study will enroll people who have recently been diagnosed with TTP or recently experienced a relapse and have not yet had six plasma exchanges during the current episode of TTP. Participants will be randomly assigned to receive either plasma exchanges and corticosteroids or plasma exchanges, corticosteroids, and rituximab. Blood will be collected from participants at baseline and each day they undergo the plasma exchange procedure. All participants will receive a plasma exchange every day until their platelet counts are normal and signs of tissue damage have improved. Participants will receive corticosteroid medication every day until plasma exchange is stopped, at which time the dosage will be gradually tapered until 7 weeks after the last plasma exchange. Participants receiving rituximab will receive the first dose intravenously within 7 days of the first plasma exchange; they will continue to receive rituximab once a week for 4 weeks. After the plasma exchanges are completed, all participants will have routine follow-up care with their doctors to make sure there is no TTP relapse. In the 1 year after study entry, additional blood collections will occur at varying times. Study researchers will monitor participants' health in the 3 years after study entry by following up with their doctors or through periodic phone calls. A portion of blood will be collected and stored for future TTP research purposes; this is optional.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2008-11-26
• Study First Submitted QC: 2008-11-26
• Study First Posted: 2008-12-01
• Study Start: 2009-04
• Primary Completion: 2010-02
• Study Completion: 2010-02
• Results First Submitted: 2013-05-07
• Status Verified: 2013-07
• Results First Submitted QC: 2013-07-18
• Last Update Submitted: 2013-07-18
• Results First Posted: 2013-07-22
• Last Update Posted: 2013-07-22

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 3

Inclusion Criteria

• Differential or admission diagnosis of TTP-like syndrome, defined as the following:

  1. Platelet count of less than 80,000/µL for newly diagnosed patients and less than 120,000/µL for relapsed patients
  2. Microangiopathic hemolytic anemia (MHA) with red blood cell fragmentation
  3. Lactate dehydrogenase (LDH) level greater than two times the upper limit of normal for newly diagnosed patients and greater than the upper limit of normal for relapsed patients

• Receiving or will receive treatment for TTP with plasma exchange

• Has not started the sixth plasma exchange in the current TTP episode

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Exclusion Criteria

• Treated for TTP in the 2 months before study entry

• Previously enrolled in this study

• Severe active infection indicated by sepsis (requirement for pressors with or without positive blood cultures) or clinical evidence of enteric infection with E. coli 0157 or related organism

• Currently under treatment for cancer or has a current diagnosis of cancer (other than localized skin carcinoma)

• Microangiopathic hemolytic anemia due to a mechanical heart valve

• Severe high blood pressure, as defined by systolic blood pressure of greater than 180 and diastolic blood pressure of greater than 120, or papilledema

• Has ever had an organ or stem cell transplant

• Has received calcineurin inhibitors (e.g., sirolimus, tacrolimus, cyclosporin A) in the 6 months before TTP diagnosis

• Diagnosis of disseminated intravascular coagulation (DIC), defined as the following:

  1. International normalized ratio (INR) level greater than 2.0 (unrelated to anticoagulation, unresponsive to vitamin K administration) OR
  2. Fibrinogen less than 100 mg/dL

• Pregnant

• Requires ventilator assistance or intravenous pressors for treatment of TTP. If no longer required prior to study entry, patient is eligible for the study.

• Known congenital TTP or family history of TTP

• Established diagnosis of lupus, and/or actively treated for lupus in the 60 days before study entry. In addition, people with two or more of the following systemic lupus erythematosus (SLE) clinical criteria in the 60 days before study entry will be excluded:

  1. Characteristic skin rash, either malar or photosensitive
  2. Symmetric polyarthritis
  3. Serositis, either pleurisy or pericarditis

• Previously received rituximab

• Has taken the following drugs known to be associated with TTP-like syndrome in the 3 months before study entry: clopidogrel (Plavix), ticlopidine (Ticlid), or quinine

• Will receive more than 1.5 plasma volumes per day after study entry

• HIV history or positive serology

• History of hepatitis B or positive serology for HBsAg or Anti-hepatitis B core antigen (Anti-HBc)

• History of hepatitis C

• Known persistent or unexplained platelet count below 150,000/µL in the 3 months before current TTP episode

• Known hypersensitivities or allergies to murine and/or humanized antibodies

• Currently participating in trials of investigational therapies or devices (other than investigational central catheters)

• Has ever had a diagnosis of ventricular tachycardia

• Acute transmural heart attack during the current hospital admission

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
1	Rituximab	Participants will receive rituximab in addition to plasma exchange and corticosteroids.
1	Plasma exchange	Participants will receive rituximab in addition to plasma exchange and corticosteroids.
1	Corticosteroids	Participants will receive rituximab in addition to plasma exchange and corticosteroids.
2	Plasma exchange	Participants will receive plasma exchange and corticosteroids.
2	Corticosteroids	Participants will receive plasma exchange and corticosteroids.

Primary Outcome Measures

Name	Time	Method
Role of Rituximab in Increasing Early Treatment Response in Participants With TTP Who Are Also Treated With Plasma Exchange and Corticosteroids	Measured at Day 52

Secondary Outcome Measures

Name	Time	Method
Use of Non-study Treatment	Measured at Month 36
Whether Participants Receiving Rituximab Achieve Early or Late Treatment Response Faster and Require Fewer Plasma Exchanges Than Participants Not Receiving Rituximab	Measured at Days 52 and 82
Relationship Between Clinical and Laboratory Data and Response to Treatment	Measured at Days 52 and 82
Incidence of Relapse Among Participants in the Two Study Groups Who Achieve Early Treatment Response	Measured at Month 36
All Cause Mortality	Measured at Month 36
Treatment-related Complications	Measured at Day 52
Evaluating How Levels of ADAMTS-13 Enzyme and Autoantibody at Specific Time Points or Over the Course of the Study Correlate With Other Indicators of Disease Activity, Remission Rates, Rapidity of Achieving a Remission, and Recurrence Rate	Measured at Month 36
Rituximab Response in Participants With Varying Levels of ADAMTS-13 Activity and Antibodies Against ADAMTS-13	Measured at Month 36
Effect of Plasma Exchange on Rituximab Levels	Measured at Month 6
Effect of Rituximab Levels on the Extent of B-cell Depletion (CD-19+ Cells)	Measured at Month 12
B-cell Depletion in Relation to ADAMTS-13 Activity and to ADAMTS-13 Antibody Levels and Disease Activity in Participants Who Receive Rituximab Versus Those Who do Not	Measured at Month 12

Trial Locations

Locations (23)

New York-Presbyterian Hospital/Weill Cornell Medical Center; 🇺🇸 New York, New York, United States

University of Iowa; 🇺🇸 Iowa City, Iowa, United States

Emory University; 🇺🇸 Atlanta, Georgia, United States

University of Alabama, Birmingham; 🇺🇸 Birmingham, Alabama, United States

Johns Hopkins Hospital; 🇺🇸 Baltimore, Maryland, United States

Gunderson Clinic, LTD; 🇺🇸 LaCrosse, Wisconsin, United States

University of Pittsburgh Presbyterian and Shadyside Hospital; 🇺🇸 Pittsburgh, Pennsylvania, United States

University of Oklahoma Health Sciences Center; 🇺🇸 Oklahoma City, Oklahoma, United States

Beth Israel Deaconess Medical Center; 🇺🇸 Boston, Massachusetts, United States

University of Maryland Medical Center; 🇺🇸 Baltimore, Maryland, United States

Massachusetts General Hospital; 🇺🇸 Boston, Massachusetts, United States

Brigham and Women's Hospital; 🇺🇸 Boston, Massachusetts, United States

Children's Hospital Boston; 🇺🇸 Boston, Massachusetts, United States

University of North Carolina Hospitals; 🇺🇸 Chapel Hill, North Carolina, United States

Puget Sound Blood Center; 🇺🇸 Seattle, Washington, United States

Duke University Medical Center; 🇺🇸 Durham, North Carolina, United States

University Hospital Cleveland; 🇺🇸 Cleveland, Ohio, United States

Integris Baptist Medical Center; 🇺🇸 Oklahoma City, Oklahoma, United States

University of Pennsylvania; 🇺🇸 Philadelphia, Pennsylvania, United States

University of Wisconsin at Madison; 🇺🇸 Madison, Wisconsin, United States

Children's Hospital of Pittsburgh; 🇺🇸 Pittsburgh, Pennsylvania, United States

Froedtert Memorial Lutheran Hospital; 🇺🇸 Milwaukee, Wisconsin, United States

Tulane University Health Sciences Center; 🇺🇸 New Orleans, Louisiana, United States