Treatment of paroxysmal nocturnal hemoglobinuria patients by an inhibitor of complement
Eculizumab, a humanized monoclonal antibody against C5 that inhibits terminal complement activation, showed activity in a preliminary 12-week open-label trial in a small cohort of patients with paroxysmal nocturnal hemoglobinuria (PNH). The present study examined whether chronic eculizumab therapy could reduce intravascular hemolysis, stabilize hemoglobin levels, reduce transfusion requirements, and improve quality of life in a double-blind, randomized, placebo-controlled, multi-center global Phase III trial. It has been found that eculizumab stabilized hemoglobin levels, decreased the need for transfusions, and improved quality of life in PNH patients via reduced intravascular hemolysis. Chronic eculizumab treatment appears to be a safe and effective therapy for PNH.
1. A method of treating a patient suffering from paroxysmal nocturnal hemoglobinuria (PNH) comprising administering to the patient a pharmaceutical composition comprising an antibody that binds C5, wherein the antibody comprises a heavy chain consisting of SEQ ID NO: 2 and a light chain consisting of SEQ ID NO: 4, and wherein the composition comprises a single-unit dosage form comprising 300 mg of the antibody in 30 mL of a sterile, preservative-free solution.
2. The method of claim 1 , wherein the patient has received at least four transfusions in the twelve months prior to administration of the antibody.
3. The method of claim 2 , wherein the patient has a platelet count greater than or equal to 100,000 per microliter prior to administration of the antibody.
4. The method of claim 3 , wherein the patient is treated with the antibody for at least 26 weeks.
5. A method of treating a patient suffering from paroxysmal nocturnal hemoglobinuria (PNH) comprising administering to the patient a pharmaceutical composition comprising an antibody that binds C5, wherein the antibody comprises a heavy chain consisting of SEQ ID NO: 2 and a light chain consisting of SEQ ID NO: 4, wherein the composition comprises a single-unit dosage form comprising 300 mg of the antibody in 30 mL of a sterile, preservative-free solution, and wherein the patient exhibits decreased lactate dehydrogenase levels.
6. The method of claim 5 , wherein the patient has received at least four transfusions in the twelve months prior to administration of the antibody.
7. The method of claim 6 , wherein the patient has a platelet count greater than or equal to 100,000 per microliter prior to administration of the antibody.
8. The method of claim 7 , wherein the patient is treated with the antibody for at least 26 weeks.