Swedish Orphan Biovitrum AB (publ)

Haemophilia A Prophylaxis and Bleeding Control

Research activity in haemophilia A centres on long-term prophylactic management, prevention of joint bleeds, and control of breakthrough bleeding in people with severe disease. The trials also examine treatment continuity in previously treated patients and comparative pharmacokinetics of extended half-life factor VIII products.

  • Prophylactic factor VIII therapy
  • Joint bleed prevention
  • Bleeding episode management
  • Pharmacokinetic assessment

Clinical interest extends to sustained treatment use across multiple countries and real-world settings, with a focus on maintaining protection against bleeding complications.

Joint Health and Musculoskeletal Outcomes

Several studies focus on joint health in haemophilia, including changes in physical activity, overall joint status, and structural findings such as synovial hypertrophy. Ultrasound is used to characterise joint involvement in patients receiving prophylaxis.

  • Physical activity over time
  • Synovial hypertrophy
  • Ultrasound-based joint assessment
  • Musculoskeletal function

This area reflects a strong therapeutic interest in preserving mobility and reducing haemophilia-related joint damage in both adolescents and adults.

Haemophilia B and Extended Prophylaxis

Research also includes haemophilia B, with attention to prophylactic treatment and joint outcomes in patients receiving long-acting factor IX replacement. These studies assess how ongoing prevention strategies relate to joint condition in routine care and follow-up settings.

  • Factor IX prophylaxis
  • Joint outcome monitoring
  • Long-acting clotting factor therapy
  • Haemophilia B care

The sponsor’s portfolio in this area links bleeding prevention with longer-term assessment of joint preservation in people living with inherited bleeding disorders.

Transplant-associated Thrombotic Microangiopathy

In transplant-associated thrombotic microangiopathy (TA-TMA), the research focus is on treatment evaluation after hematopoietic stem cell transplantation, with attention to pharmacokinetics, safety, and tolerability. This reflects an interest in severe post-transplant complications requiring specialised therapeutic management.

  • TA-TMA treatment
  • Post-transplant complications
  • Safety and tolerability
  • Pharmacokinetic evaluation

The sponsor’s activity in this field addresses a rare, high-acuity haematologic condition within the transplant setting.

Want to learn more about this study or check if you can participate? Contact us.

Matched clinical trials

  • Study on Long-Term Effects of Efanesoctocog Alfa in Preventing Joint Bleeds in Patients with Hemophilia A

    Recruiting

    3 1 1 1
    Investigated drugs:
    Croatia Czechia France Germany Ireland Italy +2
  • Continued Access Study for Patients with Severe Hemophilia A Using Efanesoctocog Alfa

    Recruiting

    3 1 1 1
    Investigated drugs:
    Bulgaria France Germany Greece Italy The Netherlands +4
  • Study on Joint Health in Hemophilia A and B Patients Using Efmoroctocog Alfa or Eftrenonacog Alfa

    Not yet recruiting

    3 1 1 1
    Bulgaria Croatia Czechia France Hungary Ireland +4
  • Study on Synovial Hypertrophy in Patients with Hemophilia A Using Efanesoctocog Alfa Prophylaxis

    Not recruiting

    3 1 1 1
    Investigated diseases:
    Investigated drugs:
    Italy Norway Spain Sweden
  • Study of Pegcetacoplan (APL-2) in Patients with Transplant-associated Thrombotic Microangiopathy After Stem Cell Transplantation

    Not recruiting

    2 1 1 1
    Investigated diseases:
    France Greece Italy Spain
  • Study on Physical Activity and Joint Health in Patients Aged 12 and Older with Severe Hemophilia A Treated with Efanesoctocog Alfa for 24 Months

    Not recruiting

    3 1 1
    Investigated drugs:
    Austria Belgium Croatia Czechia France Germany +8