A Study of Safety and Effectiveness of NovoThirteen® (rFXIII) During Treatment of Congenital FXIII Deficiency in Japan

CompletedOBSERVATIONAL
Enrollment

8

Participants

Timeline

Start Date

March 16, 2016

Primary Completion Date

September 30, 2024

Study Completion Date

September 30, 2024

Conditions
Congenital Bleeding DisorderCongenital FXIII Deficiency
Interventions
DRUG

recombinant factor XIII

No treatment given.Patients will be treated according to routine clinical practice at the discretion of the treating physician.

Trial Locations (8)

466-8560

Nagoya University Hospital_Blood Transfusion, Aichi

443-8501

Gamagori Hospital, Gamagori-shi, Aichi

720-0001

Chugoku Central Hospital, Hiroshima

737-0023

Kure Medical Center and Chugoku Cancer Center, Kure-shi, Hiroshima

051-8501

Nikko Memorial Hospital, Muroran, Hokkaido,

330-8777

Saitama Children's Med Centre_Hematology-Oncology, Saitama

520-1121

Takashima Municipal Hospital, Shiga

167-0035

Ogikubo Hospital_Pediatries & Blood, Tokyo

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Novo Nordisk A/S

INDUSTRY