TerminatedPhase 4NCT05856266
An 18-month Low-interventional Study to Assess Joint Health in Haemophilia A and B Patients on Prophylaxis With Efmoroctocog Alfa or Eftrenonacog Alfa
Studying Hemophilia A
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Swedish Orphan Biovitrum
- Principal Investigator
- Stefan Lethagen, MD, PhDSwedish Orphan Biovitrum AB (publ)
- Intervention
- Haemophilia Early Arthropathy Detection with Ultrasound (HEAD-US)(procedure)
- Enrollment
- 10 enrolled
- Eligibility
- 6 years · All sexes
- Timeline
- 2023 – 2023
Study locations (30)
- Study site 100, Sofia, Bulgaria
- Study site 101, Sofia, Bulgaria
- Study site 102, Zagreb, Croatia
- Study site 103, Zagreb, Croatia
- Study site 108, Brno, Czechia
- Study site 107, Liberec, Czechia
- Study site 104, Olomouc, Czechia
- Study site 105, Prague, Czechia
- Study site 106, Prague, Czechia
- Study site 115, Bordeaux, France
- Study site 129, Caen, France
- Study site 125, Chambéry, France
- Study site 110, Clermont-Ferrand, France
- Study site 123, Dijon, France
- Study site 124, Lille, France
- +15 more locations on ClinicalTrials.gov
Collaborators
IQVIA Pvt. Ltd
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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