WHO ICTRP trial

A 24 month, multi-center, open-label, randomized, controlled study to evaluate…

NL-OMON37144 · Overview of Medical Research in the Netherlands (NL-OMON) · Not Recruiting

Key facts

Trial ID NL-OMON37144
Public title A 24 month, multi-center, open-label, randomized, controlled study to evaluate the efficacy and safety of concentration controlled everolimus to eliminate or to reduce tacrolimus compared to tacrolimus in de novo liver transplant recipients.
Scientific title A 24 month, multi-center, open-label, randomized, controlled study to evaluate the efficacy and safety of concentration controlled everolimus to eliminate or to reduce tacrolimus compared to tacrolimus in de novo liver transplant recipients. - Evaluation of efficacy and safety of Certican versus…
Primary sponsor Novartis
Registry Overview of Medical Research in the Netherlands (NL-OMON)
Recruitment status Not Recruiting
Study type Interventional
Phase 3
Countries Netherlands
Conditions Impaired renal function after liver transplantation;10019654;10038430;Impaired renal function after liver transplantation
Interventions Group 1 (elimination arm): low dose Prograft until month 4 (then elimination) + Certican + steroids Group 2 (minimalisation arm): low dose Prograft + Certican + steroids Group 3 (control arm): standard treatment Prograft + steroids…
Registration date Nov 1, 2011
Target size 30
Secondary IDs 2007-001821-85;NL20355.078.07
Registry page onderzoekmetmensen.nl

At a glance

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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