drugset / Trial / NCT01708564

A Phase I Safety, Pharmacokinetics and Pharmacodynamics Study of Recombinant Factor VIIa in Adult Patients With Hemophilia A or B

NCT01708564

Phase 1 Completed 15 enrolled rEVO Biologics
Non-randomizedSingle-groupOpen-labelBasic science

Summary

This study will assess the pharmacokinetics and pharmacodynamics of rhFVIIa at three dose levels. The results will help identify the most optimal doses to take forward to the Phase 2/3 studies where bleedings in hemophilia patients with inhibitors will be treated with rhFVIIa.

Timeline

Start
2012-10
Primary completion
2013-06
Completion
2013-06

Drugs

EvaluationDrugModalityDoseRoute
Subject eptacog alfa (activated) Protein / enzyme biologic 25 ug/kg
Subject eptacog alfa (activated) Protein / enzyme biologic 75 ug/kg
Subject eptacog alfa (activated) Protein / enzyme biologic 225 ug/kg

Indications