Skip to content

Multicenter study of combination therapy using mizoribine, cyclosporin, basiliximab and steroids in kidney transplantation.

Multicenter study of combination therapy using mizoribine, cyclosporin, basiliximab and steroids in kidney transplantation. - Multicenter study of combination therapy using mizoribine, cyclosporin, basiliximab and steroids in kidney transplantation.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000000732
Enrollment
70
Registered
2007-06-10
Start date
2006-06-01
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

Kidney transplantation

Interventions

cyclosporinbasiliximab + steroids + mizoribine

Sponsors

MNKT Forum
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.living donor kidney transplantation. 2.Gender free, any case of uremia. 3.Aged 2 years to 70 years. 4.ABO compatible (including semi-compatible) The patient or whose family has submitted (if the patient is showing disturbance of consciousness or decreased ability to understand) written consent forms based on their free choice once adequate information and understandings are obtained regarding the study upon the participation.

Exclusion criteria

Exclusion criteria: 1.The patient who has a history of hypersensitivity against components of either one of the following drugs: Bredinin tablet, Neoral or Simulect. 2.The patient who is pregnant or a female patient who is expecting to become pregnant. 3.The patients who showed a positive result with cross match test. 4.The patient who recived ABO incompatible donor. 5.The patient with whom the physician-in-charge considered inappropriate as a subject of this study.

Design outcomes

Primary

MeasureTime frame
Incidence of virus infection

Secondary

MeasureTime frame
Rejection reactions (incidence, types, severity), patient survival rate, graft suvival rate, incidence of adverse events / abnormalities in the laboratory values.

Countries

Japan

Outcome results

None listed

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