drugset / Trial / NCT01228669

Safety of NNC 0172-0000-2021 in Healthy Male Subjects and Subjects With Haemophilia A or B

NCT01228669

Phase 1 Completed 52 enrolled Novo Nordisk A/S
RandomizedSingle-groupDouble-blindTreatment

Summary

This trial is conducted in Europe and Asia. The aim of this clinical trial is to investigate the safety, pharmacokinetics (how the trial drug is distributed in the body) and pharmacodynamics (physiological effects of the drug on the body) of NNC 0172-0000-2021 administered intravenously and subcutaneously to healthy male subjects and subjects with haemophilia A or B

Timeline

Start
2010-10-25
Primary completion
2012-09-10
Completion
2012-09-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Concizumab Monoclonal antibody 0.5 ug/kg Intravenous
Subject Concizumab Monoclonal antibody 50 ug/kg Intravenous
Subject Concizumab Monoclonal antibody 3000 ug/kg Intravenous
Subject Concizumab Monoclonal antibody 9000 ug/kg Intravenous