Safety, Tolerability, and Pharmacokinetics Study of Turoctocog Alfa Pegol Injected Under the Skin in Patients With Haemophilia A

Completed · Phase 1

Conditions studied: Congenital Bleeding Disorder, Haemophilia A

In brief

The trial is conducted in Asia, Europe and North America. The aim of the study is to evaluate the safety of administration under the skin of turoctocog alfa pegol (SC N8-GP) in patients with severe haemophilia A.

Key facts

Study ID

NCT02994407

Run by

Novo Nordisk A/S

People needed

50

Starts

2017-01-30

Expected to finish

2018-10-15

Last updated by the study team

2020-02-05

Who can join

Age: 12 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Male, age above or equal to 18 years at the time of signing informed consent,(part A).
• Male, age above or equal to 12 years at the time of signing informed consent,(part B).
• Diagnosis of congenital haemophilia A based on medical records (FVIII activity <1%).
• History of more than 150 exposure days to any FVIII containing products.

You may not qualify if…

• Previous participation in this trial. Participation is defined as signed informed consent.
• (Patients who have completed part A are allowed to also participate in part B. If so, a separate informed consent covering part B must be signed.)
• Immune compromised patients due to human immunodeficiency virus (HIV) infection (defined as viral load greater than or equal to 400.000 copies/mL and/or cluster of differentiation 4+ (CD4+) lymphocyte count less than or equal to 200/μL performed at screening or defined by medical records no older than 6 months)
• Any history of FVIII inhibitors (defined by medical records within 8 years of randomisation)
• Inhibitors to FVIII (greater than or equal to 0.6 Bethesda unit (BU)) at screening, measured by Nijmegen modified Bethesda method at central laboratory.

Where it is running

• Novo Nordisk Investigational Site — Orlando, Florida, United States
• Novo Nordisk Investigational Site — Iowa City, Iowa, United States
• Novo Nordisk Investigational Site — East Lansing, Michigan, United States
• Novo Nordisk Investigational Site — Cleveland, Ohio, United States
• Novo Nordisk Investigational Site — Dayton, Ohio, United States
• Novo Nordisk Investigational Site — Charleston, South Carolina, United States
• Novo Nordisk Investigational Site — Norfolk, Virginia, United States
• Novo Nordisk Investigational Site — Milwaukee, Wisconsin, United States
• Novo Nordisk Investigational Site — Innsbruck, Austria
• Novo Nordisk Investigational Site — Vienna, Austria
• Novo Nordisk Investigational Site — Nantes, France
• Novo Nordisk Investigational Site — Berlin, Germany
• Novo Nordisk Investigational Site — Duisburg, Germany
• Novo Nordisk Investigational Site — Homburg, Germany
• Novo Nordisk Investigational Site — Shinjuku-ku, Tokyo, Japan
• Novo Nordisk Investigational Site — Tokyo, Japan
• Novo Nordisk Investigational Site — Belgrade, Serbia
• Novo Nordisk Investigational Site — Belgrade, Serbia
• Novo Nordisk Investigational Site — Novi Sad, Serbia

Full record on ClinicalTrials.gov

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