Shares in USA-based ViroPharma fell 5.3% to $6.23 on February 13, after the firm cancelled a Phase III trial evaluating maribavir to prevent cytomegalovirus disease in liver transplant patients. All subjects receiving the investigational drug are being moved to the current standard-of-care. The decision was based on the results of a late-stage study of the antiviral in stem-cell transplant patients, and a recommendation from its Independent Data Monitoring Committee, which considered the rate of viremia in both arms of the study. The abandoned Phase III study was a randomized, double-blind, multicenter trial intended to enroll 348 subjects. The primary efficacy endpoint was the incidence of CMV disease within six months post transplantation, which is expected to be approximately 12% in the oral ganciclovir control arm of the study, based on data from published literature.
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