IP Library Granted Patent US 12,076,376
Granted Patent B2
US 12,076,376 · App. 17/854,325 · Granted Sep 3, 2024

Methods for treating lysosomal acid lipase deficiency in patients

Inventor: Anthony Quinn (Chestnut Hill, MA)
Assignee: Alexion Pharmaceuticals, Inc.
A61K38/465A61K31/135A61K31/138A61K31/366A61K31/397A61K45/06A61P3/06C12N9/18C12N9/20C12Y301/01013
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Quick Facts
Patent No.
US 12,076,376
App. No.
17/854,325
Granted
Sep 3, 2024
Kind
B2
Abstract

The present invention provides methods of treating LAL deficiency comprising administering to a mammal a therapeutically effective amount of lysosomal acid lipase with an effective dosage frequency. Methods of improving growth and liver function, increasing LAL tissue concentration, and increasing LAL activity in a human patient suffering from LAL deficiency are also provided.

Claims (18)

1. A method of treating a human infant suffering from a lysosomal acid lipase (LAL) deficiency comprising administering to the infant 1 milligram (mg), 3 mg, or 5 mg of recombinant human LAL per kilogram (kg) body weight.

2. The method of claim 1 , wherein:

a) administration of the recombinant human LAL occurs between one time every 5 days and one time every 30 days;

b) administration of the recombinant human LAL occurs about once every 7 or 14 days; or

c) administration of the recombinant human LAL occurs by intravenous infusion or intravenous injection, optionally over a period of 1 to 8 hours.

3. A method of treating a human subject suffering from a lysosomal acid lipase (LAL) deficiency, wherein the subject is a child or an adult, comprising administering to the subject 1 mg/kg or 3 mg/kg of recombinant human LAL.

4. The method of claim 3 , wherein:

a) administration of the recombinant human LAL occurs between one time every 5 days and one time every 30 days;

b) administration of the recombinant human LAL occurs about once every 7 or 14 days; or

c) administration of the recombinant human LAL occurs by intravenous infusion or intravenous injection, optionally over a period of 1 to 8 hours.

5. A method of treating a human subject suffering from a lysosomal acid lipase (LAL) deficiency, comprising administering to the subject 1 mg/kg, 3 mg/kg, or 5 mg/kg of recombinant human LAL over a period of 1 to 8 hours by intravenous infusion.

6. The method of claim 5 , wherein:

a) administration of the recombinant human LAL occurs about once every 7 days or 14 days;

b) the subject is an infant and administration of the recombinant human LAL occurs about once every 7 days; or

c) the subject is a child or an adult and administration of the recombinant human LAL occurs about once every 14 days.

7. A method of treating a human subject suffering from a lysosomal acid lipase (LAL) deficiency, comprising:

a) administering an antihistamine to the subject; and

b) after administration of the antihistamine, administering 1 mg/kg or 5 mg/kg of recombinant human LAL to the subject.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 28, 2022
From: QUINN, ANTHONY
To: SYNAGEVA BIOPHARMA CORP.
Reel/Frame 061576/0485 →
MERGER AND CHANGE OF NAME Recorded Oct 28, 2022
From: SYNAGEVA BIOPHARMA CORP.; GALAXY MERGER SUB LLC
To: ALEXION PHARMA LLC
Reel/Frame 061576/0775 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 28, 2022
From: ALEXION PHARMA LLC
To: ALEXION PHARMACEUTICALS, INC.
Reel/Frame 061576/0825 →
Continuity (10)
Continuation 16190878 · Nov 14, 2018
Continuation 14851387 · Sep 11, 2015
Continuation 14633240 · Feb 27, 2015
Continuation 14102000 · Dec 10, 2013
Continuation 13229558 · Sep 9, 2011
Continuation In Part PCTUS2011033699 · Apr 23, 2011
Provisional Application 61432372 · Jan 13, 2011
Provisional Application 61456014 · Oct 29, 2010
Provisional Application 61403011 · Sep 9, 2010
Related Publication 20220362350A1 · Nov 17, 2022