US2020140531A1PendingUtilityA1

Methods for treating complement-associated disorders

Assignee: ALEXION PHARMA INCPriority: Nov 10, 2008Filed: Oct 11, 2019Published: May 7, 2020
Est. expiryNov 10, 2028(~2.3 yrs left)· nominal 20-yr term from priority
A61P 7/02A61P 9/00C07K 2317/24A61P 37/06A61K 39/395C07K 2317/34A61K 9/0019A61K 38/16A61P 37/02C07K 16/18A61K 38/00A61P 7/04A61P 21/04A61P 13/12A61P 43/00A61K 2039/505A61K 2039/54A61K 2039/545A61P 21/02A61P 9/12A61K 38/19A61K 45/06A61P 9/14A61K 39/3955
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Claims

Abstract

The present disclosure relates to, inter alia, compositions containing an inhibitor of human complement and use of the compositions in methods for treating or preventing complement-associated disorders. In some embodiments, the inhibitor is chronically administered to patients. In some embodiments, the inhibitor is administered to a patient in an amount and with a frequency to maintain systemic complement inhibition and prevent breakthrough. In some embodiments, the compositions contain an antibody, or antigen-binding fragment thereof, that binds to a human complement component C5 protein or a fragment of the protein such as C5a or C5b.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for treating complement-mediated thrombotic microangiopathy (TMA) in a patient, the method comprising administering eculizumab to the patient in an amount effective to treat complement-mediated TMA, wherein eculizumab is intravenously administered to the patient under the following schedule:
 at least 600 mg of eculizumab once per week for four consecutive weeks; and   beginning at week five, maintenance doses of at least 900 mg eculizumab every two weeks thereafter.   
     
     
         2 . The method of  claim 1 , wherein the eculizumab is administered to the patient in an amount and with a frequency to maintain at least 50 μg of eculizumab per milliliter of the patient's blood. 
     
     
         3 . The method of  claim 1 , wherein eculizumab is administered to the patient in an amount and with a frequency to maintain at least 100 μg of eculizumab per milliliter of the patient's blood. 
     
     
         4 . The method of  claim 1 , wherein eculizumab is administered to the patient in an amount and with a frequency to maintain a concentration of at least 0.7 molecules of eculizumab per every C5 molecule in the patient's blood.

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