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Completed Phase 3 Interventional Results available

Evaluating the Haemostatic Effect of NNC 0129-0000-1003 During Surgical Procedures in Subjects With Haemophilia A.

ClinicalTrials.gov ID: NCT01489111

Public ClinicalTrials.gov record NCT01489111. 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 Sep 12, 2026, 10:11 PM EDT

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

Official title

Efficacy and Safety of NNC 0129-0000-1003 During Surgical Procedures in Patients With Haemophilia A

Brief summary

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

This trial is conducted globally. The aim of this trial is to evaluate the haemostatic effect of NNC 0129-0000-1003 during surgical procedures in subjects with haemophilia A.

Study identification

NCT ID
NCT01489111
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
36 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years and older
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
Aug 2, 2012
Primary completion
Dec 9, 2018
Completion
Dec 9, 2018
Last update posted
Aug 9, 2020

2012 – 2018

United States locations

U.S. sites
19
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Novo Nordisk Investigational Site Phoenix Arizona 85016-7710
Novo Nordisk Investigational Site Long Beach California 90806
Novo Nordisk Investigational Site Sacramento California 95817
Novo Nordisk Investigational Site Torrance California 90502-2004
Novo Nordisk Investigational Site Orlando Florida 32827
Novo Nordisk Investigational Site Tampa Florida 33607
Novo Nordisk Investigational Site Boise Idaho 83712
Novo Nordisk Investigational Site Iowa City Iowa 52242
Novo Nordisk Investigational Site New Orleans Louisiana 70118-5720
Novo Nordisk Investigational Site Baltimore Maryland 21287
Novo Nordisk Investigational Site Newark New Jersey 07102
Novo Nordisk Investigational Site Cincinnati Ohio 452289
Novo Nordisk Investigational Site Portland Oregon 97239
Novo Nordisk Investigational Site Philadelphia Pennsylvania 19134
Novo Nordisk Investigational Site Charleston South Carolina 29425
Novo Nordisk Investigational Site Nashville Tennessee 37232-9830
Novo Nordisk Investigational Site Houston Texas 77030
Novo Nordisk Investigational Site Norfolk Virginia 23507
Novo Nordisk Investigational Site Spokane Washington 99204

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 51 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01489111, 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 Aug 9, 2020 · Synced Sep 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01489111 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →