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Trial information

A Study of CellCept (Mycophenolate Mofetil) in Combination Therapy in Heart Transplant Patients.

Status: No longer recruiting

Protocol number: ML20055

Sponsor: Hoffmann-La Roche

Company division: Pharmaceutical

Official Scientific Title: An open label study to evaluate the effect of CellCept in combination wth cyclosporine A and steroids on renal function and the prevention of acute rejection in heart transplant patients.

Brief summary: This study will investigate the efficacy and safety of CellCept (1.5-2g/day po), in combination with a standard care regimen of cyclosporine A (trough level 150-200ng/mL) and steroids, in patients receiving a heart transplant. The anticipated time on study treatment is 3-12 months, and the target sample size is <100 individuals. Target sample size is 36.

Study phase: III

Study type: Interventional; Treatment; Non-Randomized; Open Label; Uncontrolled; Single Group; Safety/Efficacy study

Condition: Heart Transplantation

Intervention type: Drug

Intervention name: mycophenolate mofetil[CellCept]

Primary outcome: 1. Renal function (calculated creatinine clearance at 24 weeks post-transplant), incidence of acute rejection or HDC, or graft loss, up to 12 months post-transplant.

Key secondary outcomes: 1. Efficacy: incidence of malignancies; incidence of infections; AEs.

Inclusion criteria:

  • adult patients, >=18 years of age;
  • patients receiving their first heart transplant (single organ transplant).

Exclusion criteria:

  • patients with a positive donor-specific cross-match at the time of transplantation;
  • patients with any antibody-treated acute rejection;
  • known contraindications to treatment with sirolimus;
  • history of malignancy, other than excised non-melanoma skin cancer which has not recurred for 2 years.

Gender: Males or Females

Age limits: Min: 18 Years Max: N/A (No limit)

Accepts healthy volunteers: No

Anticipated start date: August, 2006

Trial registration date: 07/19/2006

Date last updated: 8/29/2008


Link to trial result

This trial was conducted at the following locations:

China

  • Beijing
  • Fuzhou
  • Shanghai

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