Trial Information

Summary: A Study of CellCept (Mycophenolate Mofetil) in Combination Therapy in Liver Transplant Patients.

Status: Recruiting

Protocol Number: ML21273

Sponsor: Hoffmann-La Roche

Company Division: Pharmaceutical

Official Scientific Title: A randomized, open label study comparing the effect of CellCept with therapeutic drug monitoring, tacrolimus and a corticosteroid-sparing regimen versus fixed dose CellCept, tacrolimus and corticosteroids maintained up to 6 months, on acute rejection and safety in liver transplant patients.

Brief Summary: This 2 arm study will compare the efficacy and safety of two CellCept-containing treatment regimens in de novo liver transplant patients. Patients will be randomized into one of two groups, to receive either CellCept (at a starting dose of 3g/day po, adjusted according to exposure) standard dose tacrolimus and corticosteroids (10-15 mg/kg i.v. on day 0), or fixed dose CellCept 2g/day po, standard dose tacrolimus and corticosteroids (10-15mg/kg i.v. on day 0, then reducing from 20mg to 5mg over 6 months, and discontinuing after 6 months). The anticipated time on study treatment is 3-12 months, and the target sample size is 100-500 individuals. Target sample size is 250.

Study Phase: IV

Study Design / Study Details:

  • Purpose: Treatment
  • Allocation: Randomized
  • Masking: Open Label
  • Control: Active
  • Assignment: Parallel
  • Endpoints: Safety/Efficacy

Study Type:

Interventional

Condition: Liver Transplantation

Intervention Type: Drug

Intervention Name: mycophenolate mofetil [CellCept]

Primary Outcome: 1. Incidence of biopsy-proven and treated acute rejection Time frame: Up to month 12

Key Secondary Outcomes: 1. Patient and graft survival; histological evaluation of grafts. Time frame: Month 12 2. Cardiovascular outcomes and renal function Time frame: Month 12 3. AEs, laboratory parameters. Time frame: Throughout study

Inclusion Criteria:

  • adult patients, >=18 years of age;
  • recipient of a first orthotopic liver transplant.

Exclusion Criteria:

  • history of organ transplants;
  • patient receiving a multi-organ transplant;
  • calculated creatinine clearance <=30mL/min before transplant;
  • leukocyte count < 2000/mm3 at randomization;
  • history of cancer within past 5 years, except for successfully treated basal cell or squamous cell cancer, or in situ cervical cancer;
  • pregnant or breast-feeding females, or females of childbearing age not using effective contraception.

Gender: Males or Females

Age Limits: Min: 18 Years

Accepts Healthy Volunteers: No

Anticipated Start Date: October, 2007

Trial Registration Date: 10/15/2007

Date Last Updated: 08/18/2008

Link To Trial Results

Contact:

Research Site:
Located In:
Paris, France, 75018
Telephone: 973-235-5000 or 800-526-6367

 

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Trial listings updated: September 2, 2008 at 1:55:11 PM


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