drugset / Trial / NCT00886353

Safety and Tolerability Study of APN01 (Recombinant Human Angiotensin Converting Enzyme 2)

NCT00886353 ↗

Phase 1 Completed 22 enrolled Apeiron Biologics
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

EvaluationDrugModalityDoseRoute
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