drugset / Trial / NCT01454986

Study to Evaluate Safety, Tolerability, PK and PD of ALXN1007 in Healthy Subjects

NCT01454986 ↗

Phase 1 Completed 64 enrolled Alexion Pharmaceuticals, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of the study is to evaluate the safety, tolerability, PK and PD of a single-dose of ALXN1007 in healthy volunteers.

Timeline

Start
2011-11
Primary completion
2013-08
Completion
2013-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator OLENDALIZUMAB Monoclonal antibody 0.06 mg/kg Intravenous
Comparator OLENDALIZUMAB Monoclonal antibody 0.1 mg/kg Intravenous
Comparator OLENDALIZUMAB Monoclonal antibody 0.3 mg/kg Intravenous
Comparator OLENDALIZUMAB Monoclonal antibody 1 mg/kg Intravenous
Comparator OLENDALIZUMAB Monoclonal antibody 3 mg/kg Intravenous
Comparator OLENDALIZUMAB Monoclonal antibody 6 mg/kg Intravenous
Comparator OLENDALIZUMAB Monoclonal antibody 10 mg/kg Intravenous

Indications

No indication recorded.