Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to: - 1. To evaluate the tolerability and safety of infusing reduced volume Factor Eight Inhibitor Bypassing Activity (FEIBA) at the standard infusion rate of 2 U/kg/min - 2. To evaluate the tolerability and safety of infusing reduced volume FEIBA at increased rates of 4 and 10 U/kg/min, in comparison to the standard rate of 2 U/kg/min at the regular volume


Clinical Trial Description

15 JUN 2020: The temporary enrollment stop of new patients into this study due to the COVID-19 pandemic has been lifted in one or more countries/sites, and the study is now again enrolling new patients. However, some countries/sites may still have paused the enrollment of new patients due to the pandemic. 23 APRIL 2020: Enrollment of new patients into this study has been paused due to the COVID-19 situation. The duration of this pause is dependent on the leveling and control of the COVID-19 pandemic. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02764489
Study type Interventional
Source Takeda
Contact
Status Completed
Phase Phase 3
Start date February 12, 2019
Completion date December 27, 2021

See also
  Status Clinical Trial Phase
Completed NCT00851721 - Efficacy and Safety Study of Prophylactic Versus On-Demand Treatment With Feiba NF in Subjects With Hemophilia A or B and a High Titer Inhibitor Phase 3
Completed NCT02919800 - A Single-dose, Dose-escalation Study of a Long-acting MOD-5014 in Healthy Adult Male Phase 1