Post-Marketing Surveillance (All Case Surveillance) on Treatment With Alhemo® in Patients With Haemophilia A or Haemophilia B With Inhibitors

Enrolling by invitationOBSERVATIONAL
Enrollment

23

Participants

Timeline

Start Date

August 8, 2024

Primary Completion Date

April 30, 2030

Study Completion Date

April 30, 2030

Conditions
Haemophilia AHaemophilia B
Interventions
DRUG

Concizumab

Participants will be treated with commercially available Alhemo (Concizumab) according to routine clinical practice at the discretion of the treating physician. The decision to initiate treatment with commercially available Concizumab has been made by the participant/ legally acceptable representative (LAR) and the treating physician before and independently from the decision to include the participant in this study.

Trial Locations (7)

Unknown

Novo Nordisk Investigational Site, Toshima City

035-8601

Mutsu general hospital, Aomori

812-8582

Kyushu university hospital_Pediatrics, Fukuoka

004-0041

Sapporo Tokushukai Hospital_Pediatrics, Hokkaido

890-8760

Kagoshima City Hospital, Kagoshima

216-8511

St. Marianna University School of Medicine Hospital_Pediatrics, Kanagawa

160-0023

Tokyo Medical University Hospital, Tokyo

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Novo Nordisk A/S

INDUSTRY