drugset / Trial / NCT00886353
Safety and Tolerability Study of APN01 (Recombinant Human Angiotensin Converting Enzyme 2)
RandomizedSingle-groupQuadruple-blindTreatment
Summary
The purpose of this study is to define the dose for a Phase II study and to investigate safety and tolerability of intravenous administration of recombinant soluble human Angiotensin Converting Enzyme 2 in healthy volunteers.
Timeline
- Start
- 2009-04
- Primary completion
- 2009-11
- Completion
- 2009-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | GSK2586881 | Protein / enzyme biologic | 100 ug/kg | Intravenous |
| Comparator | GSK2586881 | Protein / enzyme biologic | 200 ug/kg | Intravenous |
| Comparator | GSK2586881 | Protein / enzyme biologic | 400 ug/kg | Intravenous |
| Comparator | GSK2586881 | Protein / enzyme biologic | 800 ug/kg | Intravenous |