Trials / Completed
CompletedNCT00481481
Conversion Study From Cyclosporine to FK506MR Based Immunosuppression in Kidney Transplant Subjects
A Multicenter, Single-arm, Open, Conversion Study From a Cyclosporine (CyA) Based Immunosuppressive Regimen to a Tacrolimus Modified Release, FK506E (MR4), Based Immunosuppressive Regimen in Kidney Transplant Subjects (CONCERTO: Converting Cyclosporine to FK506E (MR4) in Renal Transplantation)
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 346 (actual)
- Sponsor
- Astellas Pharma Inc · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Assessment of the safety and the efficacy of a tacrolimus modified release (FK506MR) based immunosuppressive regimen in stable kidney transplant subjects converted from a cyclosporin based immunosuppressive regimen.
Detailed description
Multicenter, single-arm, open phase IIIb, conversion study where a Cyclosporine A-based immunosuppressive regimen is replaced by the administration of tacrolimus modified release formulation, MR4, once daily (morning dosing only) in stable renal transplant subjects. The initial recommended dose of MR4 is 0.1 mg/kg/day. Twenty-four weeks of treatment on MR4-based immunosuppressive regimen is considered to be an appropriate study duration in order to assess the response in subjects suffering from one or more known cyclosporine side effects, hypertrichosis/hirsutism, gingival hyperplasia, hyperlipidemia, arterial hypertension. Stable, adult kidney transplant recipients (≥ 12 months post transplant) who are currently treated with cyclosporine and who meet the Inclusion and Exclusion Criteria will be enrolled.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | tacrolimus | immunosuppression |
Timeline
- Start date
- 2007-04-01
- Primary completion
- 2009-04-01
- Completion
- 2009-04-01
- First posted
- 2007-06-01
- Last updated
- 2014-07-18
Locations
56 sites across 13 countries: Austria, Belgium, Czechia, Denmark, Finland, France, Germany, Hungary, Italy, Poland, Spain, Sweden, Switzerland
Source: ClinicalTrials.gov record NCT00481481. Inclusion in this directory is not an endorsement.