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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 below
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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:
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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 weeks
Treatment ~ Varies
Follow Up ~one month post completion
This trial's timeline: 3 weeks for screening, Varies for treatment, and one month post completion for reporting.

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 more

Awards & 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.

Find a Location

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

Daratumumab (Monoclonal Antibodies) Clinical Trial Eligibility Overview. Trial Name: NCT05300451 — Phase 2
Heart Transplant Research Study Groups: HLA Desensitization Group
Heart Transplant Clinical Trial 2023: Daratumumab Highlights & Side Effects. Trial Name: NCT05300451 — Phase 2
Daratumumab (Monoclonal Antibodies) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05300451 — Phase 2
~1 spots leftby Aug 2025