Efficacy and Safety of RBCs Derived From Mirasol-treated Whole Blood in Patients Requiring Chronic Transfusion (PRAISE) (PRAISE)
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| ClinicalTrials.gov Identifier: NCT03329404 |
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Recruitment Status :
Terminated
(Study suspended due to blood supply challenges. Subsequently approved by FDA to reopen but will not do so because of changing clinical need.)
First Posted : November 6, 2017
Results First Posted : April 28, 2021
Last Update Posted : April 28, 2021
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Transfusion Dependent Thalassemia | Device: Mirasol Red Blood Cells (MIR RBCs) Device: Reference Red Blood Cells (REF RBCs) | Not Applicable |
Patients will be randomized 1:1 to receive either Mirasol-treated RBCs followed by conventional RBCs, or to receive conventional RBCs followed by Mirasol-treated RBCs. The blood centers will collect the donor RBCs and supply the Mirasol-treated RBCs to the hospital sites for transfusion into patients. Hospital sites will order conventional RBCs as per their normal process, from their standard vendor.
Blood transfusion is the mainstay of care for individuals with thalassemia major. The purpose of transfusion is twofold: to improve the anemia and to suppress the ineffective erythropoiesis. A transfusion episode for these thalassemia patients are the routine transfusions administered on a regular schedule for the life of the patient.
The crossover trial design will consist of 2 treatment periods. Each period will include a 50 day wash-in phase (Day 0 of the wash-in = Day 0 of the treatment period) followed by 2 transfusion episodes. An end of study treatment follow-up visit will occur 2-4 weeks after the last per protocol transfusion, prior to the next standard of care transfusion. A final study visit will occur at least 60 days after the last per protocol transfusion.
The primary objective of the PRAISE study is to determine if percent survival of RBCs derived from Mirasol-treated WB is non-inferior to conventional RBCs when transfused into patients requiring chronic RBC transfusion support. The secondary objectives include comparing other efficacy and safety endpoints between treatment groups.
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 12 participants |
| Allocation: | Randomized |
| Intervention Model: | Crossover Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | Evaluate the Efficacy and Safety of RBCs Derived From Mirasol-treated Whole Blood Compared With Conventional RBCs in Patients Requiring Chronic Transfusion Support |
| Actual Study Start Date : | April 23, 2018 |
| Actual Primary Completion Date : | December 19, 2018 |
| Actual Study Completion Date : | December 19, 2018 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Mirasol Red Blood Cells (MIR RBCs)
MIR RBCs: RBCs will be derived from WB collected in CPD solution, treated with the Mirasol System for WB, LR, and stored in AS-3 for ≤ 21 days at 1-6°C
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Device: Mirasol Red Blood Cells (MIR RBCs)
Mirasol Red Blood Cells (MIR RBCs) derived from Mirasol-treated WB; WB will be Mirasol treated, centfifuged and leukoreduced and the derived RBCs will be stored before transfusion for up to 21 days and transfused according to the patient's transfusion schedule. |
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Active Comparator: Reference Red Blood Cells (REF RBCs)
Reference Red Blood Cells (REF RBCs); LR apheresis RBCs or WB-derived RBCs will be per site standard inventory
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Device: Reference Red Blood Cells (REF RBCs)
Reference Red Blood Cells (REF RBCs) will be acquired from routine use inventory and transfused according to the patient's transfusion schedule. |
- Normalized Hemoglobin (Hb AUC) Calculated From Normalized Hb Between Successive Transfusions as a Measure of Percent Surviving RBCs [ Time Frame: Crossover design with 2 treatment periods. Each period included a 50-day wash-in followed by 2 transfusion episodes for primary endpoint assessment. Expected participation was approximately 7-10 months, depending on the subject's transfusion schedule. ]The Hb AUC is calculated using the trapezoidal method on normalized Hb. The normalization is accomplished by dividing all posttransfusion Hb values by the 15-minute posttransfusion Hb level. The ratio is expressed as a percentage. A natural log-transform of the observed normalized Hb AUC will be utilized.
- Hb Increment [ Time Frame: An average of 30 weeks consisting of 2 crossover treatment periods with each period including a 50 day wash-in phase followed by 2 transfusion episodes for endpoint assessment ](post-transfusion Hb - pre-transfusion Hb)/Hb transfused]/RBC volume in subject at pre-transfusion
- Actual Hb Level Post-transfusion (15 Min) [ Time Frame: An average of 30 weeks consisting of 2 crossover treatment periods with each period including a 50 day wash-in phase followed by 2 transfusion episodes for endpoint assessment ]Actual Hb level post-transfusion (15 min)
- Proportional Decline in Post-transfusion Hb Level [ Time Frame: An average of 30 weeks consisting of 2 crossover treatment periods with each period including a 50 day wash-in phase followed by 2 transfusion episodes for endpoint assessment ]Proportional decline in post-transfusion Hb level
- RBC Mass Infused [ Time Frame: An average of 30 weeks consisting of 2 crossover treatment periods with each period including a 50 day wash-in phase followed by 2 transfusion episodes for endpoint assessment ]volume x Hb/unit
- Incidence of Treatment-emergent Antibody With Confirmed Specificity to RBCs Derived From Mirasol-treated WB [ Time Frame: Up to 40 weeks consisting of 2 crossover treatment periods with each period including a 50 day wash-in phase followed by 2 transfusion episodes for endpoint assessment and a final study visit 60 days after last study transfusion ]
- Human Leukocyte Antigen (HLA) Alloimmunization Rates [ Time Frame: An average of 15 weeks consisting of the first treatment period including a 50 day wash-in phase followed by 2 transfusion episodes ]
- Treatment Emergent Adverse Events (TEAEs). [ Time Frame: Up to 40 weeks consisting of 2 crossover treatment periods with each period including a 50 day wash-in phase followed by 2 transfusion episodes for endpoint assessment and a final study visit 60 days after last study transfusion ]
- Transfusion-related Adverse Events (AEs). [ Time Frame: Up to 40 weeks consisting of 2 crossover treatment periods with each period including a 50 day wash-in phase followed by 2 transfusion episodes for endpoint assessment and a final study visit 60 days after last study transfusion ]
- Serious Adverse Events (SAEs). [ Time Frame: Up to 40 weeks consisting of 2 crossover treatment periods with each period including a 50 day wash-in phase followed by 2 transfusion episodes for endpoint assessment and a final study visit 60 days after last study transfusion ]
- Unanticipated Adverse Device Effects (UADEs). [ Time Frame: Up to 40 weeks consisting of 2 crossover treatment periods with each period including a 50 day wash-in phase followed by 2 transfusion episodes for endpoint assessment and a final study visit 60 days after last study transfusion ]
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 12 Years and older (Child, Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
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1. Transfusion dependent thalassemia patient with mean 2-4 week transfusion intervals for the prior 6 months.
2. Age ≥ 12 years.
3. Negative pregnancy test for women of childbearing potential and agreement to practice a medically acceptable contraception regimen throughout the participation in the clinical trial. Not required if female subjects are not of child-bearing potential (ie, prior to menses onset, surgically sterilized, 1-year postmenopausal).
4. Signed informed consent from the patient, or if the patient is < 18 years of age, signed assent from patient and consent from parent/guardian, according to local Institutional Review Board/Ethics Committee (IRB/EC) requirements.
Exclusion Criteria:
- Historical RBC transfusion requirement of more than 250 mL/kg/year.
- Presence of RBC antibodies that make procurement of compatible RBC units not feasible per the treating physician's clinical judgment for reasonable execution of the study.
- Prior treatment with pathogen-reduced RBCs with subsequent development of known antibodies to the associated RBCs.
- Planned treatment requirement of frozen RBC products.
- Treatment requirements for any medication that is known to cause hemolysis.
- Receiving cardiac medications for heart failure.
- Patients anticipated to receive massive transfusion, per the treating physician's clinical judgment.
- Known HIV infection (defined as HIV RNA positive) with changes to antiviral regimen within the 12 months prior to screening.
- Acute or chronic medical disorder that, in the opinion of the Investigator, would impair the ability of the patient to receive study treatment.
- Participation in another clinical study, either concurrently or within the previous 28 days, in which the study drug or device may influence study endpoints or patient safety, according to Investigator discretion.
- Participation in another clinical study within the past 3 months if investigational RBCs or treatment or drugs were received that are likely to have long term effect on RBCs function.
- Pregnant or breastfeeding.
- Planned concurrent treatment with other pathogen reduction treated blood products during participation in this study.
- Patients who received prior treatment with pathogen-reduced RBCs within the past 120 days.
- Inability to comply with study procedures and/or follow-up.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03329404
| United States, California | |
| UCSF Benioff Children's Hospital Oakland | |
| Oakland, California, United States, 94609 | |
| United States, Massachusetts | |
| Boston Children's Hospital | |
| Boston, Massachusetts, United States, 02116 | |
| United States, New York | |
| Weill-Cornell Medical College | |
| New York, New York, United States, 10065 | |
| United States, Pennsylvania | |
| The Children's Hospital of Philadelphia | |
| Philadelphia, Pennsylvania, United States, 19104 | |
| Israel | |
| Rambam Health Care Campus | |
| Haifa, Israel, 3109601 | |
| Hadassah Ein Kerem Hospital | |
| Jerusalem, Israel, 91120 | |
| Italy | |
| Centro della Microcitemia ed Anemie Congenite Ospedale Gallieria | |
| Genova, Genoa, Italy, 16128 | |
| U.O.C. di Ematologia e Malattie Rare del Sangue e degli Organi Ematopoietici V. Cervello Hospital | |
| Palermo, Italy, 90146 | |
| Turkey | |
| Ege University Children's Hospital | |
| Bornova, Izmir, Turkey, 35040 | |
| Study Director: | Ned Cosgriff, MD | Terumo BCT | |
| Principal Investigator: | Steve Sloan, MD, PhD | Boston Children's Hospital |
Documents provided by Terumo BCTbio:
| Responsible Party: | Terumo BCTbio |
| ClinicalTrials.gov Identifier: | NCT03329404 |
| Other Study ID Numbers: |
CTS-5056 |
| First Posted: | November 6, 2017 Key Record Dates |
| Results First Posted: | April 28, 2021 |
| Last Update Posted: | April 28, 2021 |
| Last Verified: | December 2019 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | Yes |
| Device Product Not Approved or Cleared by U.S. FDA: | Yes |
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Thalassemia pathogen reduction therapy |
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Thalassemia Anemia, Hemolytic, Congenital Anemia, Hemolytic Anemia |
Hematologic Diseases Hemoglobinopathies Genetic Diseases, Inborn |