INTERCEPT Blood System for RBCs Study in Regions at Potential Risk for Zika Virus Transfusion-Tra… (NCT03037164) | Clinical Trial Compass
Active — Not RecruitingPhase 3
INTERCEPT Blood System for RBCs Study in Regions at Potential Risk for Zika Virus Transfusion-Transmitted Infections
United States692 participantsStarted 2017-05-11
Plain-language summary
To evaluate the safety and efficacy of red blood cells (RBCs) prepared with the INTERCEPT Blood System for Red Blood Cells Pathogen Reduction Treatment (PRT) in comparison to conventional RBCs in patients who require RBC transfusion support.
Who can participate
Age range4 Years
SexALL
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Inclusion Criteria:
* Age ≥ 4 years.
* Patients who require or are expected to require a transfusion of RBC component(s), including red cell exchange transfusion
* Signed and dated informed consent form.
* Female patients of child-bearing potential must:
* Have negative serum or urine pregnancy tests performed at the Screening visit within 30 days of randomization to rule out pregnancy, and
* Agree to use to use at least one method of birth control that results in a low failure rate (i.e., less than 1% per year) when used consistently and correctly such as implants, injectables, combined oral contraceptives, some intrauterine devices (IUDs), sexual abstinence or vasectomized partner for the duration of study participation and an additional 28 days.
For 28-day +6-month extension study in patients requiring repeated simple transfusions:
• A diagnosis of a bone marrow failure syndrome requiring repeated RBC transfusion for congenital or acquired chronic anemia (e.g., sickle cell anemia, thalassemia, other hemoglobinopathies, myelodysplastic syndrome, aplastic anemia, chemotherapy or stem cell transplant etc.)
For 28-day +6-month extension study in SCD patients requiring regular repeated RCE.
* Diagnosis of SCD, either HbSS, HbSC or HbSB0 thalassemia, confirmed by Hb electrophoresis, deoxyribonucleic acid (DNA) analysis or high-performance liquid chromatography (HPLC)
* Currently participating in an automated RCE transfusion program (for at least 3 months prior to enrol…