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Clinical trial intelligence report
A Multi-Center, Phase II Trial of HLA-Mismatched Unrelated Donor Bone Marrow Transplantation With Post-Transplantation Cyclophosphamide for Patients With Hematologic Malignancies
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT02793544-Jul 28, 2026
NCT ID
NCT02793544
Status
COMPLETED
Phase
Phase 2
Sponsor
Center for International Blood and Marrow Transplant Research
Executive brief
Investment-Ready Snapshot
This Phase II trial, sponsored by the Center for International Blood and Marrow Transplant Research, explores the efficacy of HLA-mismatched unrelated donor bone marrow transplantation in patients with hematologic malignancies. The trial's completion in March 2020 positions it favorably for potential market entry, particularly in the context of increasing demand for alternative donor sources in hematopoietic cell transplantation. The competitive landscape includes established therapies for hematologic malignancies, but the unique approach of utilizing mismatched donors may provide a niche advantage. Diligence should focus on the trial's safety and efficacy data, particularly regarding GVHD incidence and overall survival rates, to assess market viability and reimbursement potential.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02793544
Indication
Myelodysplastic Syndrome (MDS)
Modality
small molecule
Target
HLA-mismatched unrelated donor bone marrow transplantation with post-transplantation cyclophosphamide (PTCy), sirolimus, and mycophenolate mofetil (MMF) for graft versus host disease (GVHD) prophylaxis.
Intervention
Fludarabine, Cyclophosphamide 14.5 mg/kg/day IV on Days -6, -5, Total Body Irradiation (TBI) 200cGy on Day -1, Infusion of non-T-cell depleted bone marrow on Day 0, Busulfan, Cyclophosphamide 50mg/kg/day IV on Days -2,-1, Cyclophosphamide 50mg/kg/day IV on Days -5,-4, Total Body Irradiation (TBI) 200cGy twice a day on Days -3, -2, -1, Post-HCT Cyclophosphamide 50mg/kg IV on Day+3, +4, Sirolimus, Mycophenolate mofetil, G-CSF, Pre-HCT Mesna on Days -6 and -5, Pre-HCT Mesna on Days -2 and -1, Pre-HCT Mesna on Days -5 and -4, Post-HCT Mesna
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.