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Study identifier: NCT04631211 Synced from ClinicalTrials.gov · July 28, 2026
● Terminated

Thrombosomes® in Bleeding Thrombocytopenic Patients Study

Condition: Thrombocytopenia · Hematologic Malignancy · Bone Marrow Aplasia  ·  Sponsor: Cellphire Therapeutics, Inc.

PhasePhase 2
Planned participants21
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This prospective, multicenter, randomized, open-label, Phase 2, parallel, dose ranging, multidose trial will enroll patients into 3 Thrombosomes dose groups and 1 control liquid stored platelets (LSP) group in order to evaluate, in a dose-escalation manner, the safety, and impact on bleeding, and the preliminary effect on coagulation measures of increasing doses of allogeneic Thrombosomes in comparison to standard of care, LSP.

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

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Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (6)

City of HopeDuarte, California, United States
Medstar GeorgetownWashington D.C., District of Columbia, United States
Vanderbilt University Medical CenterNashville, Tennessee, United States
MD Anderson Cancer CenterHouston, Texas, United States
Rambam Medical CenterHaifa, Israel
Helse Bergen Haukeland University HospitalBergen, Norway

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Source record: clinicaltrials.gov/study/NCT04631211