Biotin-Acridine Red Cell Exchange Kinetics
- Conditions
- Sickle Cell Disease
- Registration Number
- NCT07155031
- Lead Sponsor
- Cerus Corporation
- Brief Summary
The primary objective of the study is to describe the recovery and survival of pathogen-reduced (PR) red blood cells (RBCs) prepared and stored with the INTERCEPT Blood System for RBCs® (hereafter referred to as INTERCEPT RBCs) in patients with sickle cell disease (SCD) undergoing red cell exchange (RCE) therapy, utilizing flow cytometry for biotin and acridine RBC surface markers.
- Detailed Description
This trial is designed as a prospective, Phase 2, non-randomized, open-label, single arm, single center study in at least five (5) patients with sickle cell disease (SCD) undergoing red cell exchange (RCE) therapy.
Subjects receiving routine care for SCD utilizing regular RCE therapy at Grady Memorial Healthcare will be approached by Emory investigators and asked to enroll in the trial. Interested subjects will complete an informed consent form (ICF) and undergo pre-study screening, including a test for the presence of naturally-occurring antibodies with specificity for INTERCEPT RBCs and for antibodies with specificity for biotin. Subjects with a positive screen for INTERCEPT RBC antibodies or for biotin antibodies will be excluded from the study. Investigators will screen the current pool of patients receiving RCE treatment at Grady Memorial Healthcare to identify at least five (5) subjects who meet the study's enrollment criteria.
Enrolled and consented subjects will receive a full unit of INTERCEPT RBCs following each of two sequential RCE episodes (RCE #1 and RCE #2). The INTERCEPT RBCs will be administered by simple transfusion immediately following the end of each RCE. During RCE #1 subjects will also receive two biotinylated aliquots (\~7 ml each) of RBCs drawn from the full INTERCEPT RBC unit before and after the PR process. The volume of each transfused aliquot will be assessed by weighing the syringe before and after transfusion. Each aliquot will be labeled at different biotin concentrations: (6 or 18 μg) to allow differentiation by flow cytometry. Subjects will be followed through a total of 4 sequential RCE episodes. Subjects will receive a full unit of INTERCEPT RBCs following RCE #2, with no biotinylated aliquots. No additional INTERCEPT RBCs will be transfused during RCE #3 or RCE #4.
To measure RBC recovery and blood volume, subject blood samples will be collected at the following time points:
* RCEs #1 and #2
* Day 0: pre-RCE and at 15, 30, and 60 minutes post-RCE.
* Days 1, 2-4, 7
* Day 14 post-RCE #1 (no Day 14 sample after RCE #2).
* RCEs #3 and #4
o Day 0: Fifteen minutes to 1 hour before and after the completion of each RCE episode.
* Appx Day 180 (±15 days) End of Study
Subjects will be screened for treatment-emergent antibodies to INTERCEPT RBCs and to biotinylated RBCs at screening and on day 14 post-RCE #1, Day 7 post-RCE #2, prior to RCE #3 and RCE #4 and on Day 180 (±15 days) post-RCE #1.
Subject RBC samples will be frozen and batched for flow-cytometry analysis at Cerus Corporation. De-glycerolized previously frozen RBCs will be used flow cytometry assessments. The assay to detect biotin levels by flow cytometry will use avidin- Allophycocyanin (APC) labeling in combination with an anti-acridine antibody. Acridine levels on INTERCEPT RBCs will be detected by flow cytometry utilizing a monoclonal antibody specific to the acridine moiety found on INTERCEPT RBCs. The antibody signal will be resolved in the phycoerythrin (PE) channel. QuantiBRITE PE beads (QB-PE) will be used to generate quasi-quantitative data for acridine RBC surface antigen labelling.
Subjects will be monitored closely during the blood transfusion procedure by staff trained to detect adverse events with transfusion. Laboratory monitoring for events of special interest will occur for 4 weeks (for hemolytic transfusion reactions) after RCE#1.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 5
- Age ≥18 years
- homozygous sickle cell disease (HbSS) or Hemoglobin S-β-thalassemia (HbSβ0) SCD
- Receiving RCE for ≥3 months prior to enrollment and scheduled to undergo at least 4 sequential RCE episodes during the period of enrollment in the study
- Anticipated cessation of RBC transfusion therapy in the next ≤2 months
- Planned stem cell transplant or gene therapy in the next 6 months
- Delayed hemolytic transfusion reaction in the past 3 months
- History of hyperhemolysis syndrome at any time
- Consuming high-dose biotin or raw egg supplements
- Current pregnancy
- Antibody specific to INTERCEPT RBCs or biotinylated red blood cells (BioRBCs) at baseline
- Patients with RBC alloantibodies that make it difficult to provide antigen matched blood.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Recovery 24 hour The volume of distribution and 24-hour post transfusion recovery (PTR24) of the INTERCEPT RBC units
Correlation between the biotin and acridine markers 6 months Correlation between the biotin and acridine markers for determining the number of circulating INTERCEPT RBCs
Survival 6 months Comparison of Pre-PR and INTERCEPT RBC PTR24, and survival over the duration of the study with intervening RCE procedures
Acridine loss 6 months Kinetics of acridine loss from the INTERCEPT RBC surface
- Secondary Outcome Measures
Name Time Method Adverse Events 6 months All subjects will be monitored for adverse events and transfusion reactions according to standard operating procedures at the RCE site
Treatment emergent antibodies 6 months Safety assessments will also include screening for treatment emergent antibodies with specificity for INTERCEPT RBCs and for biotinylated RBCs on day 14 post-RCEs #1, Day 7 post-RCE #2, prior to RCE #3 and RCE #4 and on Day 180 (±15 days) post-RCE #1