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Monoclonal Antibodies
Daratumumab for Heart Transplant Rejection
Phase 2
Waitlist Available
Led By Barry Boilson, MD
Research Sponsored by Barry A. Boilson
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Negative pregnancy test (if woman of childbearing potential)
Be older than 18 years old
Must not have
Inability to give informed consent
History of any lymphoproliferative disorder
Timeline
Screening 3 weeks
Treatment Varies
Follow Up one month post completion
Awards & highlights
All Individual Drugs Already Approved
No Placebo-Only Group
Summary
This trial is testing a drug combination called daratumumab/hyaluronidase-fihj (DARZALEX Faspro™) to help people waiting for a heart transplant who have high levels of HLA antibodies. The drug works by targeting specific immune cells to lower these antibodies, making it easier to find a compatible donor and reducing the risk of transplant rejection.
Who is the study for?
This trial is for heart transplant patients or candidates with high HLA antibodies. Participants must have a stable neutrophil count, liver function within certain limits, and adequate kidney function. It's not open to individuals with severe lung conditions like COPD, pregnant or breastfeeding women, those with HIV or hepatitis B/C unless treated successfully, recent major cardiac events, uncontrolled heart issues including arrhythmias, severe asthma in the past 2 years, or prior use of daratumumab.
What is being tested?
The study tests DARZALEX Faspro™ (daratumumab/hyaluronidase-fihj) for its effectiveness in reducing HLA antibodies in people awaiting heart transplants and those who've received a transplant but are experiencing antibody mediated rejection due to high levels of these antibodies.
What are the potential side effects?
Potential side effects may include immune system reactions such as infusion-related responses and possible impacts on blood cell counts. Organ inflammation could occur given that it targets specific cells involved in the body's immune response.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am not pregnant or have confirmed it with a test.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am unable to understand and agree to the study's details.
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I have had a condition where my lymphocytes grow abnormally.
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I have a history of cancer.
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I have had moderate to severe asthma in the last 2 years.
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I am unable to understand and give consent for treatment.
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I have a history of HIV or hepatitis B/C.
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My lung function is less than half of what is expected for someone my age and size.
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I have a serious heart condition.
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I am on the list for both heart and liver transplants.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ one month post completion
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~one month post completion
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Effect of daratumumab therapy on HLA antibody titers in sensitization (pre-transplant)
Effect of daratumumab therapy on human leukocyte antibody (HLA) titers in resistant antibody mediated rejection (AMR)
Secondary study objectives
Effect of daratumumab on Cardiac Systolic Strain in HLA sensitized patients
Effect of daratumumab on Left Ventricular Filling Pressure Ratio in HLA sensitized patients
Effect of daratumumab on Right Ventricular Systolic Pressure (RVSP) in HLA sensitized patients
+2 moreAwards & Highlights
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: HLA Desensitization GroupExperimental Treatment1 Intervention
Subjects awaiting cardiac transplantation with high levels of circulating Human Leukocyte Antigen (HLA) antibodies will receive daratumumab/hyaluronidase-fihj.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for heart transplant patients often involve immunosuppressive therapies that target specific immune cells to prevent organ rejection. Daratumumab/hyaluronidase-fihj, for example, targets CD38 to deplete plasma cells and reduce HLA antibody levels, which is crucial in preventing antibody-mediated rejection.
Other treatments include monoclonal antibodies like rituximab, which targets CD20 on B cells, and immunosuppressive drugs like cyclophosphamide. These therapies are vital for heart transplant patients as they help prevent the immune system from attacking the transplanted heart, thereby improving graft survival and overall patient outcomes.
T Follicular Helper Cells As a New Target for Immunosuppressive Therapies.Single dose anti-CD4 monoclonal antibody for induction of tolerance to cardiac allograft in high- and low-responder rat strain combinations.
T Follicular Helper Cells As a New Target for Immunosuppressive Therapies.Single dose anti-CD4 monoclonal antibody for induction of tolerance to cardiac allograft in high- and low-responder rat strain combinations.
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Who is running the clinical trial?
Janssen Biotech, Inc.Industry Sponsor
29 Previous Clinical Trials
18,843 Total Patients Enrolled
Barry A. BoilsonLead Sponsor
Barry Boilson, MDPrincipal InvestigatorMayo Clinic
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am unable to understand and agree to the study's details.I have had a condition where my lymphocytes grow abnormally.I haven't had any cancer except for skin cancer in the last 5 years.I have had moderate to severe asthma in the last 2 years.I am unable to understand and give consent for treatment.I have a history of cancer.I have a history of HIV or hepatitis B/C.My lung function is less than half of what is expected for someone my age and size.I have a serious heart condition.I am not pregnant or have confirmed it with a test.My liver tests are within the required range.I have heart inflammation, poor heart function, and treatments haven't worked.I have not used daratumumab or similar drugs recently.I am on the list for both heart and liver transplants.
Research Study Groups:
This trial has the following groups:- Group 1: HLA Desensitization Group
Awards:
This trial has 2 awards, including:- All Individual Drugs Already Approved - Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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