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Completed Phase 3 Interventional Results available

Safety and Efficacy of Turoctocog Alfa in Previously Treated Male Children With Haemophilia A

ClinicalTrials.gov ID: NCT01138501

Public ClinicalTrials.gov record NCT01138501. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 29, 2026, 5:10 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Centre, Open-Label, Non-Controlled Trial on Safety and Efficacy of N8 in Previously Treated Paediatric Patients With Haemophilia A

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This trial is conducted in Asia, Europe, and North and South America. The aim of this clinical trial is to investigate the safety and efficacy of turoctocog alfa (recombinant factor VIII, rFVIII (N8)) in male previously treated paediatric subjects with haemophilia A.

Study identification

NCT ID
NCT01138501
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
65 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Up to 11 Years
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 2010 (Type not available)
Primary completion
Nov 2011 (Actual)
Completion
Nov 2011 (Actual)
Last update posted
Mar 17, 2017

2010 – 2011

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
Novo Nordisk Investigational Site Phoenix Arizona 85016-7710 —
Novo Nordisk Investigational Site Orange California 92868 —
Novo Nordisk Investigational Site Torrance California 90502-2004 —
Novo Nordisk Investigational Site Tampa Florida 33607 —
Novo Nordisk Investigational Site Augusta Georgia 30912 —
Novo Nordisk Investigational Site Iowa City Iowa 52242 —
Novo Nordisk Investigational Site Boston Massachusetts 02115 —
Novo Nordisk Investigational Site Detroit Michigan 48201 —
Novo Nordisk Investigational Site East Lansing Michigan 48823 —
Novo Nordisk Investigational Site Kansas City Missouri 64108-4619 —
Novo Nordisk Investigational Site Omaha Nebraska 68198-2168 —
Novo Nordisk Investigational Site Brooklyn New York 11201-5425 —
Novo Nordisk Investigational Site Valhalla New York 10595 —
Novo Nordisk Investigational Site Dayton Ohio 45404 —
Novo Nordisk Investigational Site Portland Oregon 97239-3098 —
Novo Nordisk Investigational Site Charleston South Carolina 29425 —
Novo Nordisk Investigational Site Fort Worth Texas 76104 —
Novo Nordisk Investigational Site Houston Texas 77030 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01138501, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 17, 2017 · Synced Oct 29, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01138501 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →