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Clinical Trial Summary

The prospective observational study is to establish a registry database to evaluate the potential impact of prior treatment with CMX001 on the long-term incidence of specific events, such as outcomes, late CMV and other Double-stranded DNA virus associated events, s well as survival rates in subjects previously enrolled in selected clinical studies of CMX001. Each Registry participant will be followed for a period of approximately 3 years from their enrollment in the Registry.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02167685
Study type Observational [Patient Registry]
Source Chimerix
Contact
Status Terminated
Phase
Start date January 2014
Completion date May 10, 2019

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