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NCT04584892: THIRd

Turoctocog Alfa in Haemophilic Italian Patients: Protection and Engagement in Recreational Activities

Completed Last updated 28 November 2023
What this trial tests

trial testing Turoctocog alfa in Haemophilia A in 18 participants. Completed in 27 March 2023.

Timeline
12 April 2021
Primary endpoint
27 March 2023
27 March 2023

Quick facts

Lead sponsorNovo Nordisk A/S
StatusCompleted
Study typeOBSERVATIONAL
Enrollment18
Start date12 April 2021
Primary completion27 March 2023
Estimated completion27 March 2023
Sites10 locations across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Novo Nordisk A/S — full company profile →

Who can join

12 and older, any sex, with Haemophilia A. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a study on Italian patients with haemophilia A in prophylaxis treatment with Turoctocog alfa under routine clinical conditions. The purpose of the study is to investigate the therapeutic scheme in a population of patients treated with Turoctocog alfa and to investigate the participation in recreational activities, the level of physical activity, and quality of life. Participants will get NovoEight® (Turoctocog alfa) as prescribed to them by the study doctor. The study will last for about 12 months. Participants will be requested to fill in the Questionnaires investigating the participation in recreational activities, the level of physical activity, and quality of life.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Turoctocog alfa

Trials testing the same drug.

Other recruiting trials for Haemophilia A

Currently open trials in the same condition.

Other Novo Nordisk A/S trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04584892.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing