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Clinical Trial Summary

The purpose of the study was to evaluate the efficacy of ASP0113 compared with placebo as measured by a primary composite endpoint of overall mortality and CMV end organ disease (EOD) through 1 year post-transplant. Safety of ASP0113 in participants undergoing allogeneic HCT will also be evaluated.


Clinical Trial Description

Participants will be followed for 5.5 years post-transplant for long-term safety via an annual telephone contact. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01877655
Study type Interventional
Source Astellas Pharma Inc
Contact
Status Completed
Phase Phase 3
Start date September 11, 2013
Completion date March 1, 2022