Post-marketing Surveillance (Use Result Surveillance) With Refixia®

Enrolling by invitationOBSERVATIONAL
Enrollment

20

Participants

Timeline

Start Date

August 23, 2019

Primary Completion Date

September 30, 2025

Study Completion Date

September 30, 2025

Conditions
Haemophilia B
Interventions
DRUG

Refixia®

Patients will be treated with commercially available Refixia® according to routine clinical practice at the discretion of the treating physician

Trial Locations (17)

Unknown

Novo Nordisk Investigational Site, Søborg

466-8560

Nagoya University Hospital_Blood Transfusion, Aichi

260-8677

Chiba University Hospital_Diabetes, Metabolism and Endocrinology, Chiba-shi, Chiba

654-0047

Hyogo prefectural kobe children's hospital, Hyōgo

300-0395

Tokyo Medical University Ibaraki Medical Center_Ibaraki, Ibaraki

216-8511

St. Marianna University School of Medicine Hospital_Pediatrics, Kanagawa

252-0375

Kitasato University Hospital, Kanagawa

807 8555

Hospital of the University of Occupational And Environmental Health Japan, Pediatrics, Kitakyusyu-shi, Fukuoka

371-8511

Gunma University Hospital, Dept. of Hematology, Maebashi-shi, Gunma

902-8511

Naha City Hospital, Naha-shi, Okinawa

634-8522

Nara Medical University Hospital_Pediatrics, Nara

663 8051

The Hospital of Hyogo College of Medicine_Haematology, Nishinomiya-shi, Hyogo

330-8777

Saitama Children's Med Centre_Hematology-Oncology, Saitama

773-8502

Tokushima Red Cross Hospital_Pediatrics, Tokushima

160-0023

Tokyo Medical Univ. Hospital_Laboratory Medicine, Tokyo

167-0035

Ogikubo Hospital_Tokyo, Tokyo

992-0035

Ishiyama Clinic, Yamagata

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Novo Nordisk A/S

INDUSTRY

NCT03875547 - Post-marketing Surveillance (Use Result Surveillance) With Refixia® | Biotech Hunter | Biotech Hunter