drugset / Trial / NCT01708564
A Phase I Safety, Pharmacokinetics and Pharmacodynamics Study of Recombinant Factor VIIa in Adult Patients With Hemophilia A or B
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 | — |