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Trial information

A Study to Assess Use of Zenapax (Daclizumab) and CellCept (Mycophenolate Mofetil) to Improve Kidney Function in Kidney Transplant Patients

Status: Completed

Protocol number: M67005

Sponsor: Hoffmann-La Roche

Company division: Pharmaceutical

Official Scientific Title: A randomized, open-label study comparing the effects of low-dose cyclosporine vs cyclosporine withdrawal on renal function in kidney transplant patients treated with CellCept and daclizumab

Brief summary: This study will compare kidney function in kidney transplant patients following treatment with various combinations of Zenapax, CellCept, corticosteroids, and Neoral (Cyclosporine). The anticipated time on study treatment is 6-12 months, and the target sample size is 500+ individuals. Target sample size is 525.

Study phase: III

Study type: Interventional; Treatment; Randomized; Open Label; Active; Parallel; Safety/Efficacy study

Condition: Kidney Transplantation

Intervention type: Drug

Intervention name: mycophenolate mofetil [CellCept]

Primary outcome: 1. Renal function (as measured by GFR) Time frame: 12 months post-transplant

Key secondary outcomes: 1. Patient and graft survival Time frame: 12 months post-transplant 2. Proportion of patients with biopsy-proven rejection; treatment failure. Time frame: 6 and 12 months post-transplant 3. AEs, OIs, malignancies, deaths Time frame: Throughout study

Inclusion criteria:

  • adult patients greater than 18 years of age
  • recipients of primary kidney transplant
  • single-organ recipients (kidney only)

Exclusion criteria:

  • previous treatment with Zenapax
  • history of malignancy (except localized skin cancer)

Gender: Males or Females

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

Accepts healthy volunteers: No

Trial registration date: 05/23/2005

Date last updated: 9/29/2008


Link to trial result

This trial was conducted at the following locations:

Australia

  • Adelaide
  • Sydney

Belgium

  • Bruxelles
  • Leuven

Canada

  • Calgary, AB
  • Edmonton, AB
  • Vancouver, BC
  • Saskatoon, SK

France

  • Vandoeuvre-Les-Nancy

Germany

  • Berlin
  • Hannover
  • Muenster

Mexico

  • Mexico City
  • Monterrey

Norway

  • Oslo

Poland

  • Warszawa
  • Wroclaw

Spain

  • Barcelona
  • Córdoba
  • Malaga
  • Santander
  • Valencia

Sweden

  • Goeteborg
  • Malmoe

United Kingdom

  • Birmingham
  • Glasgow
  • Leicester

United States

  • Birmingham, AL
  • San Francisco, CA
  • Livingston, NJ
  • Philadelphia, PA
  • Charleston, SC
  • Falls Church, VA

To contact Roche for more information on this trial please complete the email form below. Treatment decisions and/or suitability for a specific trial are decisions only your healthcare provider can make. If you are patient interested in any of the studies, please have your healthcare provider contact us via this website, and they will be provided with the relevant clinical trial information.

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