Phase 2
N=10
Complement Inhibition Using Eculizumab to Overcome Platelet Transfusion Refractoriness in Patients With Severe Thrombocytopenia
Thrombocytopenia · Alloimmune Platelet Refractoriness
Bottom Line
View on ClinicalTrials.gov: NCT02298933 ↗Enrolled (actual)
10
Serious AEs
60.0%
Results posted
Jan 2019
Primary outcome: Primary: Number of Subjects With Sustained Platelet Transfusion Responsiveness — 4 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Eculizumab (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- National Heart, Lung, and Blood Institute (NHLBI)
- Primary completion
- Aug 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Subjects With Sustained Platelet Transfusion Responsiveness |
4 | — |
Summary
Background:
- Platelets are tiny cells in the blood that help stop bleeding. Thrombocytopenia happens when people do not have enough normal platelets. Getting a transfusion of another person s platelets can help stop too much bleeding. But because these cells are from other people, the body may reject them,putting them at risk for serious bleeding complications. This conditions is called alloimmune platelet refractoriness . There are evidence that in many patients, platelet counts fail to increase after a platelet transfusion because the transfused platelets are destroyed by the body s defence soldier, called complement . Researchers want to see if a drug, that inhibits complement, can help increase platelet levels and reduce bleeding
Objectives:
- To see if eculizumab increases platelet levels more after a transfusion. To see if it reduces the chance of bleeding too much.
Eligibility:
- Adults 18-75 years old who have thrombocytopenia and alloimmune platelet refractoriness.
Design:
* Participants will be screened with medical history, physical exam, and blood tests.
* Participants will have the procedures listed below. They can have them while they are in the hospital. Or they can go to the outpatient clinic for them. Each visit may take up to 3 hours.
* Participants will get a meningitis vaccine if needed. Then they will get the study drug as an infusion.
* Participants will have a platelet transfusion. Their blood will be drawn every 24 hours until the platelet count is less than 10,000 per 1 microliter of blood.
* They will take antibiotics for 14 days.
* Participants will have a checkup and blood drawn twice a week for 2 weeks. They will get more transfusions if needed.
Eligibility Criteria
- INCLUSION CRITERIA:
- Ages 18-75 years inclusive.
- Ability to comprehend the investigational nature of the study and provide informed consent.
- Thrombocytopenia (due to congenital causes, bone marrow failure, hematologic malignancies, and treatment related), defined as <10k/uL without bleeding or <30K/uL with evidence of life threatening bleeding (intracranial hemorrhage, GI bleeding, pulmonary hemorrhage, uncontrolled epistaxis, hematuria).
- Diagnosed with immune platelet refractoriness, characterized by all of the following:
- Lack of adequate post-transfusion platelet count increment, defined by, CCI <7500/ul at 10-60 min, and CCI <5000/ul at 18-24 hrs (in those who had a CCI at 10-60 min greater than or equal to 5000/microl)after at least 2 consecutive transfusions.
- Presence of anti-HLA class A and/or B antibody.
EXCLUSION CRITERIA
- Active meningococcal infection.
- Severe psychiatric illness. Mental deficiency sufficiently severe as to make making informed consent impossible.
- Positive pregnancy test for women of childbearing age within 1 week.
- HIV positive test within 3 months
- Paroxysmal Nocturnal Hemoglobinuria (PNH) disease with evidence of intravascular hemolysis.
- Presence ITP/autoimmune thrombocytopenia
- Immune platelet refractoriness responsive to treatment with IVIG
RE-ENROLLMENT CRITERIA:
- Meet response criteria to the initial treatment or second treatment
- Meets all initial inclusion/exclusion criteria
Data sourced from ClinicalTrials.gov (NCT02298933). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.