Swedish Orphan Biovitrum Ab ((GB:0MTD)) announced an update on their ongoing clinical study.
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Swedish Orphan Biovitrum Ab is conducting a long-term study titled ‘A Low-interventional Study to Evaluate Long-term Effectiveness of Real-world Prophylactic Treatment With Efanesoctocog Alfa on Joint Health in People With Haemophilia A (ALTITUDE)’. The study aims to assess the effectiveness of efanesoctocog alfa in preventing joint bleeds in patients with Hemophilia A, providing valuable insights into its real-world application.
The intervention being tested is efanesoctocog alfa, a drug intended to prevent joint bleeds in individuals with Hemophilia A. Participants will receive this treatment as part of their standard care, without additional provision from the sponsor.
The study is designed as a Phase 4 interventional trial with a single-group model and no masking. Its primary purpose is treatment-focused, aiming to evaluate the drug’s long-term effectiveness in a real-world setting.
The study began on April 16, 2025, with the latest update submitted on October 2, 2025. These dates mark the study’s progress and ensure that stakeholders are informed of its current status and developments.
This study could significantly impact Swedish Orphan Biovitrum’s stock performance and investor sentiment by demonstrating the effectiveness of efanesoctocog alfa, potentially setting it apart in the competitive hemophilia treatment market.
The study is currently recruiting, with further details available on the ClinicalTrials portal.