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Non-Interventional Study of NovoSeven® Used in Patients With Haemophilia A and B With Inhibitors Under Normal Clinical Practice

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Novo Nordisk

Status

Completed

Conditions

Haemophilia B With Inhibitors
Haemophilia A With Inhibitors
Congenital Bleeding Disorder

Treatments

Drug: eptacog alfa (activated)

Study type

Observational

Funder types

Industry

Identifiers

NCT01579955
F7-1947

Details and patient eligibility

About

This study is conducted in Japan. The aim of this non-interventional study is to investigate the safety and effectiveness of treatment with eptacog alpha (NovoSeven®) under normal clinical practice conditions.

Enrollment

321 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with haemophilia A and B with inhibitors who received eptacog alpha (NovoSeven®) as treatment

Exclusion criteria

  • Patients who was not deemed to be appropriate to the treatment of eptacog alpha (NovoSeven®)

Trial design

321 participants in 1 patient group

eptacog alpha users
Treatment:
Drug: eptacog alfa (activated)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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