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Completed Phase 3 Interventional Results available

Evaluation of Recombinant Factor XIII for Prevention of Bleeding in Patients With FXIII Inherited Deficiency

ClinicalTrials.gov ID: NCT00713648

Public ClinicalTrials.gov record NCT00713648. 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 Jul 23, 2026, 3:22 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, Single-Arm and Multiple Dosing Trial on Efficacy and Safety of Monthly Replacement Therapy With Recombinant Factor XIII (rFXIII) in Subjects With Congenital Factor XIII Deficiency

Study identification

NCT ID
NCT00713648
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
41 participants

Conditions and interventions

Interventions

  • catridecacog Drug

Drug

Eligibility (public fields only)

Age range
6 Years and older
Sex
All
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
Jul 31, 2008
Primary completion
Mar 31, 2010
Completion
Mar 31, 2010
Last update posted
Feb 23, 2017

2008 – 2010

United States locations

U.S. sites
11
U.S. states
10
U.S. cities
11
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 Tampa Florida 33607
Novo Nordisk Investigational Site Atlanta Georgia 30322
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 Minneapolis Minnesota 55404
Novo Nordisk Investigational Site Columbus Ohio 43205
Novo Nordisk Investigational Site Oklahoma City Oklahoma 73104
Novo Nordisk Investigational Site Seattle Washington 98104

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 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00713648, 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 Feb 23, 2017 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00713648 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →