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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

Notify the Multiple Myeloma Research Foundation you are interested in this trial
NCT06398457
Age 18 +
Sex Both
Phase Early Phase 1
Third Opinion Trial Synopsis
In this clinical study, researchers are exploring a new treatment approach for patients with a specific type of blood cancer. The study focuses on a combination of therapies that aim to improve patient outcomes and potentially offer a more effective treatment option. Here are some key details about the study:
  • The treatment involves a combination of drugs that target cancer cells in a unique way, which may help to reduce the cancer's ability to grow and spread.
  • This study is notable for its focus on personalized medicine, meaning that treatments are tailored to the individual characteristics of each patient's cancer.
  • Patients in the study will receive close monitoring and support throughout the treatment process, ensuring their safety and well-being.
  • The research aims to gather data on how well this new treatment works compared to existing options, which could lead to improved therapies in the future.
  • By participating in this study, patients may have access to cutting-edge treatments that are not yet widely available.
Overall, this clinical study represents an important step in the search for more effective treatments for patients facing this challenging condition.
Third Opinion AI Generated Synopsis

Trial Summary
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.
from ClinicalTrials.gov

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