
C3G and primary IC-MPGN are estimated to affect 5,000 people in the US and up to 8,000 in Europe

Approximately 7,700 people in England are living with the genetic bleeding disorder

The factor VIII replacement therapy has been authorised to treat and prevent bleeding in children and adults

There are currently no treatments that target the underlying cause of C3G or IC-MPGN

The rare bleeding disorder affects approximately one in every 5,000 male births annually

The rare bleeding disorder affects approximately one in every 5,000 male births annually

The therapy’s weekly dosing has a half-life of up to four times longer than current factor VIII therapies

The C3 therapy can now be used as a first-line treatment for paroxysmal nocturnal haemoglobinuria

The rare genetic condition reduces production of factor VIII, an essential protein for blood clotting

Immune thrombocytopenia is estimated to affect up to 100 people per million

The deal includes an investigational therapy being evaluated in myelofibrosis

The rare blood cancer affects approximately one in every 500,000 people worldwide