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Clinical Trial Summary

The purpose of this study was to evaluate the efficacy of ASP0113 compared to placebo in reducing the incidence of cytomegalovirus (CMV) viremia in CMV-seronegative subjects receiving a kidney from a CMV-seropositive donor. This study also evaluated the safety of ASP0113 in this patient population.


Clinical Trial Description

Participants were followed for one year after first study drug injection. This was the primary study period. Participants were followed for 4.5 years after completion of the primary study to assess long-term safety of the vaccine. ;


Study Design


Related Conditions & MeSH terms

  • Kidney Transplantation Cytomegalovirus (CMV) Negative Recipients

NCT number NCT01974206
Study type Interventional
Source Astellas Pharma Inc
Contact
Status Completed
Phase Phase 2
Start date November 20, 2013
Completion date November 5, 2020