Descriptive Study for Turoctocog Alfa Treatment Regimen in Iraqi Haemophilia A Patients - An Observational Retrospective Study

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Drug
Study Type: Observational
SUMMARY

The study has descriptive purposes, with aim of assessing how turoctocog alfa is used in the everyday practice and to provide a baseline for the management of haemophilia A and does not involve any change in the clinical management of participants. Data will be extrapolated from the existing paper based medical records and uploaded to an electronic database specifically created for the study. Baseline information/history will be recorded at time of switching from previous FVIII replacement therapy to turoctocog alfa from the enrolled participants and outcomes will be collected according to participants visit format.

Eligibility
Participation Requirements
Sex: Male
Healthy Volunteers: f
View:

• Paediatric and adult male patients

• On-demand and prophylactic patients with haemophilia A (any severity)

• Only previously treated patients (previous FVIII replacement therapy) will be included in the study

Locations
Other Locations
Iraq
National centre for Hamophilia
ENROLLING_BY_INVITATION
Baghdad
Novo Nordisk Investigational Site
RECRUITING
Baghdad
Basrah Haemoplhilia centre
NOT_YET_RECRUITING
Basra
Hilla Haemophilia centre
NOT_YET_RECRUITING
Hillah
Karbala Haemophilia centre
ENROLLING_BY_INVITATION
Karbala
Contact Information
Primary
Novo Nordisk
clinicaltrials@novonordisk.com
(+1) 866-867-7178
Time Frame
Start Date: 2024-11-10
Estimated Completion Date: 2025-12-01
Participants
Target number of participants: 900
Treatments
Turoctocog alfa
Participants received turoctocog alfa intravenously.
Related Therapeutic Areas
Sponsors
Leads: Novo Nordisk A/S

This content was sourced from clinicaltrials.gov