Clinical trial

A Study to Evaluate the Safety and Efficacy of Prograf/FK778 and Prograf/MMF in…

NCT00282230 · Astellas Pharma Inc, Industry · Terminated

Key facts

NCT number NCT00282230
Title A Study to Evaluate the Safety and Efficacy of Prograf/FK778 and Prograf/MMF in de Novo Kidney Transplant Recipients
Official title A Phase 2, Randomized, Open-Label, Parallel Group, Multi-Center Study to Assess the Safety and Efficacy of Prograf®/FK778 and Prograf®/MMF in De Novo Kidney Transplant Recipients
Lead sponsor Astellas Pharma Inc, Industry
Collaborators Astellas Pharma US, Inc. Industry
Status Terminated
Phase Phase 2
Study type Interventional
Conditions Kidney Transplantation
Intervention type Drug
Interventions FK778
Enrollment 150
Start date Nov 1, 2003
Completion Oct 1, 2005
First posted Jan 26, 2006
Last update posted Jun 7, 2012
Countries United States

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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