Method for preventing or treating nosocomial pneumonia

US11066461B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11066461-B2
Application numberUS-201615779189-A
CountryUS
Kind codeB2
Filing dateNov 28, 2016
Priority dateNov 30, 2015
Publication dateJul 20, 2021
Grant dateJul 20, 2021

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  1. Title

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  5. First independent claim

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Abstract

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A method for preventing or treating nosocomial diseases, e.g., diseases caused by Pseudomonas aeruginosa , is provided. The method includes administering to a susceptible human subject a specified dose of a bispecific antibody that specifically binds Pseudomonas aeruginosa Psl and PcrV.

First claim

Opening claim text (preview).

What is claimed is: 1. A method of treating a Pseudomonas aeruginosa infection in a susceptible human subject comprising administering to the subject 1500 mg or 3000 mg of a bispecific antibody that specifically binds Pseudomonas aeruginosa Psl and PcrV, wherein the bispecific antibody comprises a binding domain which specifically binds to P. aeruginosa Psl comprising a set of complementarity determining regions (CDRs): HCDR1-Psl, HCDR2-Psl, HCDR3-Psl, LCDR1-Psl, LCDR2-Psl, and LCDR3-Psl, wherein HCDR1-Psl has the amino acid sequence of SEQ ID NO: 10, HCDR2-Psl has the amino acid sequence of SEQ ID NO: 11, HCDR3-Psl has the amino acid sequence of SEQ ID NO: 12, LCDR1-Psl has the amino acid sequence of SEQ ID NO: 13, LCDR2-Psl has the amino acid sequence of SEQ ID NO: 14, and LCDR3-Psl has the amino acid sequence of SEQ ID NO: 15; and a binding domain which specifically binds to P. aeruginosa PcrV comprising a set of CDRs: HCDR1-PcrV, HCDR2-PcrV, HCDR3-PcrV, LCDR1-PcrV, LCDR2-PcrV, and LCDR3-PcrV, wherein HCDR1-PcrV has the amino acid sequence of SEQ ID NO: 2, HCDR2-PcrV has the amino acid sequence of SEQ ID NO: 3, HCDR3-PcrV has the amino acid sequence of SEQ ID NO: 4, LCDR1-PcrV has the amino acid sequence of SEQ ID NO: 6, LCDR2-PcrV has the amino acid sequence of SEQ ID NO: 7, and LCDR3-PcrV has the amino acid sequence of SEQ ID NO: 8, and wherein the subject maintains a serum concentration of the bispecific antibody of at least 1.7 μg/mL through 7 days following administration of the bispecific antibody. 2. The method of claim 1 , wherein the infection is pneumonia, bacteremia, bone infection, joint infection, skin infection, burn infection, wound infection, or any combination thereof. 3. The method of claim 2 , wherein the infection is pneumonia. 4. The method of claim 1 , wherein the subject maintains a serum concentration of the bispecific antibody of at least 1.7 μg/mL through 21 days following administration of the bispecific antibody. 5. The method of claim 1 , wherein the binding domain which specifically binds to P. aeruginosa Psl comprises an scFv comprising the amino acid sequence of SEQ ID NO:9. 6. The method of claim 1 , wherein the binding domain which specifically binds to P. aeruginosa PcrV comprises a variable heavy chain comprising the amino acid sequence of SEQ ID NO:1 and a variable light chain comprising the amino acid sequence of SEQ ID NO:5. 7. The method of claim 1 , wherein the bispecific antibody comprises (i) a heavy chain of the formula VH-CH1-H1-L1-S-L2-H2-CH2-CH3, wherein VH is an anti- P. aeruginosa PcrV heavy chain variable domain comprising the amino acid sequence of SEQ ID NO: 1; CH1 is a heavy chain constant region domain 1; H1 is a first heavy chain hinge region fragment; L1 is a first linker; S is an anti- P. aeruginosa Psl ScFv molecule comprising the amino acid sequence of SEQ ID NO: 9; L2 is a second linker; H2 is a second heavy chain hinge region fragment; CH2 is a heavy chain constant region domain-2; and CH3 is a heavy chain constant region domain-3; and (ii) a light chain of the formula VL-CL, wherein VL is an anti- P. aeruginosa PcrV light chain variable domain comprising the amino acid sequence of SEQ ID NO: 5, and CL is an antibody light chain kappa constant region or an antibody light chain lambda region. 8. The method of claim 1 wherein the infection is a nosocomial infection.

Assignees

Inventors

Classifications

  • from primates, e.g. man · CPC title

  • Antagonist effect on antigen, e.g. neutralization or inhibition of binding · CPC title

  • multispecific · CPC title

  • Antibacterial agents · CPC title

  • Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title

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Frequently asked questions

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What does patent US11066461B2 cover?
A method for preventing or treating nosocomial diseases, e.g., diseases caused by Pseudomonas aeruginosa , is provided. The method includes administering to a susceptible human subject a specified dose of a bispecific antibody that specifically binds Pseudomonas aeruginosa Psl and PcrV.
Who is the assignee on this patent?
Medimmune Ltd
What technology area does this patent fall under?
Primary CPC classification C07K16/1214. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jul 20 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).