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Haplo-MAC in Kakogawa

Study of Efficacy and Safety of Myeloablative Haploidentical Stem Cell transplantation using post-transplant cyclophosphamide for refractory hematological malignancies. - Haplo-HSCT-MAC

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs051180118
Enrollment
25
Registered
2019-03-13
Start date
2017-09-28
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hematological malignancy Lymphoma, leukemia, hematological malignancy

Interventions

HLA-haploidentical related hematopoietic stem cell transplantation with myeloablative conditioning using fludarabine 125 mg/m2, buslfan 12.8 mg/kg and cyclophosphamide 29 mg/kg, and GVHD prophylaxis u

Sponsors

Okamura Atsuo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Hematopoietic malignant tumors suitable for hematopoietic stem cell transplantation 2. Disease status; remission phase or non-remission phase 3. Age; >=16 year-old, =50% b. T-Bil = 30ml/min d. SpO2 >=95% (room air) 6. No HLA-matched related donor 7. No HLA-matched unrelated donor 8. Written informed consent

Exclusion criteria

Exclusion criteria: 1.HIV antibody positivity 2.Active multiple primary cancers 3.Active infection 4.Pregnant, unwilling to practice contraception during the study, or lactating female 5.Hypersensitivity to agents used for conditioning and GVHD prophylaxis 6.Specific HLA antibody against donor HLA 7.Administration of anticancer drugs except the study protocol within 13 days before transplantation 8. Other, determination of the attending physician

Design outcomes

Primary

MeasureTime frame
One-year survival rate following transplantation

Secondary

MeasureTime frame
Graft survival rate, incidence rate and severity of acute/chronic GVHD, incidence rate of infection, GVHD free/relapse free survival, discontinuance rate of immune-suppressive agents, Fever during day 0 and day7, adverse events

Contacts

Public ContactAtsuo Okamura

Kakogawa Central City Hospital

atsuo-okamura@kakohp.jp+81-79-451-5500

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026