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ENROLLING BY INVITATION
NCT06285071

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

Sponsor: Novo Nordisk A/S

View on ClinicalTrials.gov

Summary

The purpose of the study is to investigate the safety and effectiveness of Alhemo® in all participants under real-world clinical practice in Japan. Participants will get Alhemo® as prescribed by the study doctor. The study will last for about 2 years.

Official title: A Multi-centre, Open-label, Single-arm, Non-interventional Post-marketing Study to Investigate Safety and Clinical Parameters of Alhemo® Under Routine Clinical Practice in Japan

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

23

Start Date

2024-08-08

Completion Date

2030-04-30

Last Updated

2025-08-29

Healthy Volunteers

No

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.

Locations (7)

Novo Nordisk Investigational Site

Toshima City, Tokyo, Japan

Mutsu general hospital

Aomori, Japan

Kyushu university hospital_Pediatrics

Fukuoka, Japan

Sapporo Tokushukai Hospital_Pediatrics

Hokkaido, Japan

Kagoshima City Hospital

Kagoshima, Japan

St. Marianna University School of Medicine Hospital_Pediatrics

Kanagawa, Japan

Tokyo Medical University Hospital

Tokyo, Japan