IP Library Granted Patent US 11,767,357
Granted Patent B2
US 11,767,357 · App. 16/241,410 · Granted Sep 26, 2023

Biological therapeutics for infection-relating disorders or conditions

Inventor: Huiru Wang (Willowbrook, IL)
Assignee: B & H Biotechnologies, LLC
C07K16/1018A61K35/16A61K39/12A61K39/145A61K39/15A61K39/235A61K39/29A61K39/292A61K39/42A61K47/26C07K16/00C07K16/081C07K16/082C07K16/10C07K16/109C07K16/1027A61K2039/545C07K2317/21
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Quick Facts
Patent No.
US 11,767,357
App. No.
16/241,410
Granted
Sep 26, 2023
Kind
B2
Abstract

The present invention discloses products and the methods of uses of the products for preventing and treating infectious diseases and the disorders or conditions inducible by harmful antibodies. The harmful antibodies are induced during infection, or vaccination, or use of therapeutic antibodies. The products of the present disclosure comprise immunoglobulin products, serum or plasma, specific antibodies to viral pathogens.

Claims (15)

1. A therapeutic product for treating a patient infected by an influenza virus, comprising:

(a) an effective amount of N-acetylneuraminic acid;

(b) an effective amount of N-acetylneuraminic acid methyl ester; and

(c) at least one of serum or plasma,

wherein combination of the effective amount of N-acetylneuraminic acid and the effective amount of N-acetylneuraminic acid methyl ester with at least one of serum or plasma reduces a rate of death caused by the influenza virus by at least about 70% compared to treatment with the at least one of serum or plasma alone,

wherein the effective amount of N-acetylneuraminic acid comprises about 0.1 mg/kg to about 100 mg/kg of N-acetylneuraminic acid per kg body weight of a subject,

wherein the effective amount of N-acetylneuraminic acid methyl ester comprises about 0.1 mg/kg to about 100 mg/kg of N-acetylneuraminic acid methyl ester per kg body weight of a subject, and

wherein the serum or plasma is obtained from a healthy individual.

2. The therapeutic product of claim 1 , wherein the product comprises about 0.1 mL to 1000 mL of serum or plasma.

3. The therapeutic product of claim 1 , wherein the product comprises about 0.1 mg/mL to about 20 mg/mL or about 0.1 mg/g to about 20 mg/g of N-acetylneuraminic acid and about 0.1 mL to about 1000 mL of serum or plasma.

4. The therapeutic product of claim 1 , wherein the product is in a solution, a lyophilized form, an injectable form, an infusion, or a form conjugated to a nano-particle.

5. The therapeutic product of claim 1 , wherein the influenza virus is 2009 H1N1, B influenza, H5N1, H1N1, or H3N2.

6. The therapeutic product of claim 1 , wherein the serum or plasma is obtained from more than one healthy individual.

7. The therapeutic product of claim 1 , wherein the healthy individual is a human.

8. The therapeutic product of claim 1 , wherein the patient is a human.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 22, 2023
From: WANG, HUIRU
To: B & H BIOTECHNOLOGIES, LLC
Reel/Frame 063721/0651 →
Continuity (3)
Continuation 14775984
Provisional Application 61792888 · Mar 15, 2013
Related Publication 20190270792A1 · Sep 5, 2019