drugset / Trial / NCT03196297

A Trial Evaluating Efficacy and Safety of Prophylactic Administration of Concizumab in Patients With Severe Haemophilia A Without Inhibitors

NCT03196297

Phase 2 Completed 36 enrolled Novo Nordisk A/S
NaSingle-groupOpen-labelTreatment

Summary

This trial is conducted in Asia, Europe and the United States of America (USA). The aim of the trial is to assess the efficacy of concizumab administered s.c. (subcutaneously, under the skin) once daily in preventing bleeding episodes in patients with severe haemophilia A without inhibitors.

Timeline

Start
2017-08-16
Primary completion
2018-06-22
Completion
2020-06-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Concizumab Monoclonal antibody 0.15 mg/kg Subcutaneous
Subject Concizumab Monoclonal antibody 0.25 mg/kg Subcutaneous
Background turoctocog alfa Protein / enzyme biologic