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Study identifier: NCT06398457 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Darzalex Faspro (Daratumumab and Hyaluronidase-fihj) Before Standard Desensitization and Allogeneic Peripheral Blood Stem Cell Transplantation in Adult Patients at High-risk for Primary Graft Failure Secondary to Donor Specific Antibodies

Condition: Hematologic Malignancy · Bone Marrow Transplant Rejection · Acute Myeloid Leukemia (AML)  ·  Sponsor: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

PhaseEARLY_Phase 1
Planned participants8
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This research is being done to investigate the safety and effectiveness of Darzalex Faspro (daratumumab and hyaluronidase-fihj) (a monoclonal antibody that targets plasma cells that make antibodies) and whether it can lower donor specific antibodies (DSA) levels to low enough levels to permit patients to proceed with allogeneic peripheral blood transplant (alloBMT). Those being asked to participate have high DSA levels that puts those being asked to participate at high risk of rejecting the available donor's blood stem cells and making those being asked to participate ineligible to receive a stem cell transplant.

This description comes directly from the study's public registry record.

Talk to the study team

Christian B Gocke, MD PhD  ·  4109558839  ·  cgocke2@jhmi.edu

Amanda Stevens, MD  ·  7869994146  ·  msteve35@jhmi.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Sidney Kimmel Comprehensive Cancer Center at Johns HopkinsBaltimore, Maryland, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06398457