Treatment

Soliris® (eculizumab) is the first in a new class of therapies to inhibit terminal complement, which can reduce hemolysis, improve symptoms and reduce many of the major health complications associated with PNH.23,24

Prior to approval of Soliris, there were no therapies specifically tested and approved for the treatment of patients with PNH. Treatment was limited to symptom management through periodic blood transfusions, corticosteroid therapy, anticoagulants and, infrequently, bone marrow transplantations – a high-risk procedure.8



IMPORTANT SAFETY INFORMATION

Soliris increases the risk of meningococcal infections. Meningococcal infection may become rapidly life-threatening or fatal if not recognized and treated early

Soliris® increases the risk of meningococcal infections

  • Vaccinate patients with a meningococcal vaccine at least 2 weeks prior to receiving the first dose of Soliris; revaccinate according to current medical guidelines for vaccine use
  • Monitor patients for early signs of meningococcal infections, evaluate immediately if infection is suspected, and treat with antibiotics if necessary

The effect of anticoagulant withdrawal during Soliris treatment has not been studied. Therefore, treatment with Soliris should not alter anticoagulant management.

Soliris is generally well tolerated. The most frequent adverse events observed in clinical studies were headache, a runny nose (nasopharyngitis), back pain, nausea, and tiredness (fatigue).