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Clinical trial

Post-Marketing Surveillance (Use-results Surveillance) With Esperoct®. A Multi-centre, Prospective, Observational, Non-interventional Post-marketing Study to Investigate the Long-term Safety and Effectiveness of Esperoct® in Haemophilia A Patients Under Routine Clinical Practice Conditions in Japan

NCT04334057 is registered in ClinicalTrials.gov with Novo Nordisk A/S as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Post-Marketing Surveillance (Use-results Surveillance) With Esperoct®. A Multi-centre, Prospective, Observational, Non-interventional Post-marketing Study to Investigate the Long-term Safety and Effectiveness of Esperoct® in Haemophilia A Patients Under Routine Clinical Practice Conditions in Japan
Lead sponsor
Novo Nordisk A/S
Phase
Observational
Overall status
Completed
Start date
March 31, 2021
Completion date
January 10, 2024
Enrollment
23 (actual)
Sites
20

Conditions

As the registry lists them; a condition with its own page is linked.

haemophilia a