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Clinical Trial Summary

The purpose of this study is to determine the safety and tolerability of intravenous (IV) brincidofovir (BCV; SyB V-1901) 0.2 mg/kg, 0.3 mg/kg or 0.4 mg/kg dosed twice weekly (BIW) or 0.4 mg/kg dosed once weekly (QW) for 4 weeks in subjects with AdV, and IV BCV in subjects with CMV


Clinical Trial Description

This is a Phase IIa, open-label, multiple ascending dose confirmation, multicenter study to evaluate the safety and tolerability of intravenous Brincidofovir (BCV, SyB V-1901) 0.2 mg/kg, 0.3 mg/kg, or 0.4 mg/kg dosed BIW or 0.4 mg/kg dosed QW (Cohorts 1 to 4) in adult and pediatric subjects with AdV viremia, and IV BCV in subjects with CMV. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04706923
Study type Interventional
Source SymBio Pharmaceuticals
Contact Kohji Shimasaki
Phone +81-3-6684-6616
Email MedInfo@symbiopharma.com
Status Recruiting
Phase Phase 2
Start date August 16, 2021
Completion date September 30, 2026

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