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    - PMLiVE

    Novo Nordisk’s Alhemo approved by FDA for expanded haemophilia use

    The rare bleeding disorder affects approximately 800,000 people globally

    - PMLiVE

    Pfizer shares positive phase 3 results for haemophilia A and B therapy Hympavzi

    Around 20% and 3% of haemophilia A and B patients, respectively, develop inhibitors

    - PMLiVE

    Pfizer’s Hympavzi granted MHRA approval to treat haemophilia A and B

    More than 11,800 people were living with the genetic blood disorders in the UK in 2023/2024

    - PMLiVE

    Novo Nordisk’s haemophilia A therapy Mim8 shows promise in late-stage study

    The inherited bleeding disorder accounts for up to 85% of the 1,125,000 global haemophilia cases

    - PMLiVE

    Novo Nordisk invests $1.2bn to establish rare disease production facility in Denmark

    The site will be designed to accommodate multiple product types within rare diseases

    - PMLiVE

    Pfizer’s Hympavzi receives EC approval to treat haemophilia A and B patients

    The genetic blood disorder affects more than 800,000 people globally

    - PMLiVE

    Novo Nordisk’s Alhemo recommended by CHMP for haemophilia A and B

    The rare bleeding disorder affects approximately 1,125,000 people globally

    - PMLiVE

    Pfizer’s Hympavzi granted FDA approval to treat haemophilia in adult and paediatric patients

    More than 800,000 people globally are affected by the genetic blood disorder

    - PMLiVE

    Positive results for Sanofi’s haemophilia therapy published in The Lancet

    Fitusiran reduced annualised bleeding rates by 90% compared to control arms

    - PMLiVE

    Novo Nordisk announces positive phase 3 results for haemophilia treatment

    Haemophilia affects around 1,125,000 people globally

    - PMLiVE

    Pfizer doses first patient in investigational haemophilia drug trial

    Company is evaluating marstacimab in severe haemophilia A/B patients

    - PMLiVE

    Novo Nordisk hits pause on rival to Hemlibra for haemophilia

    Halts three studies because of safety concerns

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