Last updated on May 2019

Prospective Non-interventional Study to Evaluate the Effectiveness of Elocta Compared to Conventional Factor Products


Brief description of study

The purpose of the study is to evaluate the effectiveness of Elocta compared to conventional factor products in the prophylactic treatment of patients with haemophilia A over a 24-month prospective period. Data will also be collected for a 12 month retrospective period.

Clinical Study Identifier: NCT02976753

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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