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Sobi Reports EMA’s Validation of MAA for Efanesoctocog Alfa to Treat Haemophilia A

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Sobi Reports EMA’s Validation of MAA for Efanesoctocog Alfa to Treat Haemophilia A

Shots:

  • Efanesoctocog alfa's MAA has been accepted & validated by the EMA for haemophilia A of all ages. The application was based on the P-III study (XTEND-1) & (XTEND-Kids) paediatric study evaluating efanesoctocog alfa (qw) in 159 & 74 patients aged ≥12yrs. & <12yrs.
  • The (XTEND-1) study met 1EPs & EPs and showed prevention of bleeds & superior bleed protection over prior prophylaxis along with improvements in physical health, pain & joint health. In (XTEND-Kids) paediatric study, the trial met 1EPs with no factor VIII inhibitors detected confirming the safety profile of efanesoctocog alfa
  • Efanesoctocog alfa, a novel & investigational recombinant factor VIII therapy was approved in the US as ALTUVIIIO in 2023

Ref: PRnewswire | Image: Sobi

Related News:- Sobi to Acquire CTI BioPharma for ~$1.7B

Click here to­ read the full press release 

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Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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