EP3167888

TREATMENT OF PAROXYSMAL NOCTURNAL HEMOGLOBINURIA PATIENTS BY AN INHIBITOR OF COMPLEMENT

pending
JurisdiktionEP
Anmeldedatum15. März 2007
Erteilungsdatum29. März 2024
Veröffentlichungsnr.EP3167888
Anmeldenr.EP16195355
UPC-Verfahren11

Zusammenfassung

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.

Anmelder

ALEXION PHARMA INC [US]

Erfinder

BELL LEONARD [US]ROTHER RUSSELL P [US]EVANS MARK J [US]

Externe Quellen

Klassifikation

IPC-Klassen
A61K 31/7105A61K 38/00A61K 39/395A61K 9/00A61P 7/06C07K 16/18
CPC-Klassen
A61K 31/7105A61K 38/00A61K 39/395A61K 9/0019A61P 1/14A61P 13/02A61P 15/10A61P 17/00A61P 19/00A61P 21/00A61P 25/00A61P 25/04A61P 25/18A61P 25/20A61P 25/26A61P 25/28A61P 29/02A61P 3/00A61P 3/02A61P 31/04A61P 37/04A61P 43/00A61P 7/00A61P 7/02A61P 7/06A61P 9/12C07K 16/18
AI: Life Sciences
warum

Alexion pharma — A61K39/395 + A61P7/06. Pure antibody therapeutic.

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