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Sobi presents clinical data at WFH 2025 Comprehensive Care Summit

In This Article:

STOCKHOLM, April 23, 2025 /PRNewswire/ -- Sobi® (STO: SOBI) presents clinical data aimed at updating the global haemophilia community attending this year's WFH 2025 Comprehensive Care Summit in Dubai from the 23 – 25 April. New and updated outcomes and analyses will be presented from the XTEND phase 3clinical program testing the effectiveness of Altuvoct® (efanesoctocog alfa) treatment for haemophilia A, including updates on patients' joint health and surgical outcomes in patients.

"At WFH 2025 CCS, Sobi will present highlights from the XTEND phase 3 program and discuss the new treatment paradigm with FVIII levels in the non-haemophilia range. Sharing these clinical outcomes with the wider haemophilia community will help to ensure the latest treatment approaches are widely known and understood," said Lydia Abad-Franch, MD, MBA, Head of Research, Development, and Medical Affairs (RDMA), and Chief Medical Officer at Sobi.

Key data to be presented at WFH 2025 Comprehensive Care Summit, Dubai, UAE
Altuvoct® (efanesoctocog alfa)

 

Oral Presentations

                 .

A plain language summary of the association
between joint health and patient reported
quality of life outcomes using data from the
efanesoctocog alfa Phase 3 clinical trial in
adults and adolescents with severe
haemophilia A                                                                      .

Oral presentation: Oral FP-TH-02.5

Date: Thursday 24 April 2025

Time: 08:45 – 09:00

Location: Great Ballroom                                              .


Efanesoctocog alfa for the perioperative
management of dental surgery in
participants with severe hemophilia A: 4
years of experience during the XTEND clinical
program

Oral presentation: Oral FP-WE-01.5
Date: Wednesday 23 April

Time: 16:15 – 16:30

Location: Great Ballroom

 

Posters


SHINE study design: An interventional, open-
label, Phase 4 study investigating changes in
synovial hypertrophy in patients with
haemophilia A on efanesoctocog alfa
prophylaxis

Poster presentation: Poster PO-179

Presentation dates and times:
Wednesday 23 April / 11:00 – 11:30

Thursday 24 April / 11:00 – 11:30

Poster Networking Event: Thursday 24
April / 19:00 – 20:00


Long-term outcomes of prophylaxis with
efanesoctocog alfa in adults and adolescents
previously treated on demand: second
interim analysis of XTEND-ed

Poster presentation. Poster PP-044

Presentation dates and times:
Wednesday 23 April / 11:00 – 11:30

Thursday 24 April / 11:00 – 11:30

Poster Networking Event: Thursday 24
April / 19:00 – 20:00


Plain language summary of two-year results
of weekly efanesoctocog alfa treatment in
children with severe haemophilia A: Interim
analysis of the XTEND-ed phase 3 study

Poster presentation. Poster PP-045

Presentation dates and times:
Wednesday 23 April / 11:00 – 11:30

Thursday 24 April / 11:00 – 11:30
Poster Networking Event: Thursday 24
April / 19:00 – 20:00


Plain language summary: Efanesoctocog alfa
treatment outcomes over 3 years in adults
& adolescents with severe haemophilia
A in the long-term XTEND-ed study

Poster presentation. Poster PP-046

Presentation dates and times:
Wednesday 23 April / 11:00 – 11:30

Thursday 24 April / 11:00 – 11:30

Poster Networking Event: Thursday 24
April / 19:00 – 20:00


The A-MOVE study easily explained: the
value of regular joint assessments in
individuals with haemophilia

Poster presentation: Poster PP-043

Presentation dates and times:
Wednesday 23 April / 11:00 – 11:30

Thursday 24 April / 11:00 – 11:30

Poster Networking Event: Thursday 24
April / 19:00 – 20:00

About efanesoctocog alfa

Efanesoctocog alfa [Antihemophilic Factor (Recombinant), Fc-VWF-XTEN Fusion Protein] (formerly BIVV001) is a novel and significant part of the week factor VIII therapy. It has the potential to deliver near-normal factor activity levels for significant parts of the week, improving bleed protection in a once-weekly dose for people with haemophilia A. Efanesoctocog alfa builds on the innovative Fc fusion technology by adding a region of von Willebrand factor and XTEN® polypeptides to extend its time in circulation. It is the only therapy that has been shown to break through the von Willebrand factor ceiling, which imposes a half-life limitation on current factor VIII therapies. It was approved as ALTUVIIIO™ [Antihemophilic Factor (Recombinant), Fc-VWF-XTEN Fusion Protein-ehtl] by Sanofi in the US in February 2023.