IP Library Patent Application 18715320
Patent Application
App. No. 18/715,320

INTERLEUKIN 5 BINDING PROTEIN DOSAGE REGIMEN FOR USE IN TREATING POLYANGIITIS, HYPEREOSINOPHILIC SYNDROME, CHRONIC RHINOSINUSITIS WITH NASAL POLYPS (CRSWNP), OR CHRONIC RHINOSINUSITIS WITHOUT NASAL POLYPS (CRSSNP)

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Patent No.
US None
App. No.
18/715,320
Abstract

The present disclosure relates to pharmaceutical compositions comprising from about 100 mg to about 300 mg of an antigen binding protein which binds to IL-5. Compositions and antigen binding proteins of the disclosure are useful in the treatment of IL-5 mediated diseases, such as EGPA, HES, CRSsNP and CRSwNP, and can be administered about once every 6 months.

Claims (21)

1 .- 20 . (canceled)

21 . A method of treating an IL-5 mediated disease selected from: EGPA, HES, CRSsNP and CRSwNP comprising administering to a human subject, in need thereof an antigen binding protein which binds to IL-5, the antigen binding protein comprising a heavy chain variable region having the CDRH1 amino acid sequence shown in SEQ ID NO: 5, the CDRH2 amino acid sequence shown in SEQ ID NO: 6, and the CDRH3 amino acid sequence shown in SEQ ID NO: 7; and a light chain variable region having the CDRL1 amino acid sequence shown in SEQ ID NO: 8, the CDRL2 amino acid sequence shown in SEQ ID NO: 9, and the CDRL3 amino acid sequence shown in SEQ ID NO: 10 and which also comprises a heavy chain Fc domain having a tyrosine residue at position 252, a threonine residue at position 254 and a glutamic acid residue at position 256 and wherein an amino terminus of the heavy chain Fc domain is connected to a carboxy terminus of the heavy chain variable region, in an amount of about 100 mg to about 300 mg, about once every 6 months.

22 . A method according to claim 21 , wherein the IL-5 mediated disease to be treated is selected from: EGPA and HES, and wherein about 200 mg of the antigen binding protein is administered, about once every 6 months.

23 . A method according to claim 22 , wherein said 200 mg of the antigen binding protein is administered as two doses of 100 mg.

24 . A method according to claim 21 , wherein the IL-5 mediated disease to be treated is selected from: CRSsNP and CRSwNP, and wherein about 100 mg of the antigen binding protein is administered, about once every 6 months.

25 . A method according to claim 22 , wherein said disease is HES and said human subject has a screening blood eosinophil count of >1500 eosinophils/μL at start of treatment or they are patients already diagnosed with HES who have been already exposed to standard HES therapy and have a ≥1000 cells/μL.

26 . A method according to claim 22 , wherein said disease is EGPA which is relapsing-remitting or refractory eosinophilic granulomatosis with polyangiitis.

27 . A method according to claim 24 , wherein said disease is (i) CRSsNP and said human subject has may have such a Type 2 or eosinophilic endotype with elevated levels of eosinophils in the nasal mucosa.

28 . A method of decreasing an absolute blood eosinophil count in a subject, the method comprising:

a) identifying a subject having a condition selected from the group consisting of EGPA, HES, CRSsNP and CRSwNP and

b) administering to the subject an antigen binding protein which binds to IL-5, the antigen binding protein comprising a heavy chain variable region having the CDRH1 amino acid sequence shown in SEQ ID NO: 5, the CDRH2 amino acid sequence shown in SEQ ID NO: 6, and the CDRH3 amino acid sequence shown in SEQ ID NO: 7; and a light chain variable region having the CDRL1 amino acid sequence shown in SEQ ID NO: 8, the CDRL2 amino acid sequence shown in SEQ ID NO: 9, and the CDRL3 amino acid sequence shown in SEQ ID NO: 10 and which also comprises a heavy chain Fc domain having a tyrosine residue at position 252, a threonine residue at position 254 and a glutamic acid residue at position 256 and wherein an amino terminus of the heavy chain Fc domain is connected to a carboxy terminus of the heavy chain variable region, in an amount of about 100 mg to about 300 mg, about once every 6 months,

whereby the absolute blood eosinophil count in the subject is decreased.

29 . A pre-filled syringe comprising:

a. about 100 mg to about 300 mg of an antigen binding protein which binds to IL-5, the antigen binding protein comprising a heavy chain variable region having the CDRH1 amino acid sequence shown in SEQ ID NO: 5, the CDRH2 amino acid sequence shown in SEQ ID NO: 6, and the CDRH3 amino acid sequence shown in SEQ ID NO: 7; and a light chain variable region having the CDRL1 amino acid sequence shown in SEQ ID NO: 8, the CDRL2 amino acid sequence shown in SEQ ID NO: 9, and the CDRL3 amino acid sequence shown in SEQ ID NO: 10 and which also comprises a heavy chain Fc domain having a tyrosine residue at position 252, a threonine residue at position 254 and a glutamic acid residue at position 256 and wherein an amino terminus of the heavy chain Fc domain is connected to a carboxy terminus of the heavy chain variable region; and

b. a pharmaceutically acceptable excipient.

for use in the treatment of an IL-5 mediated disease selected from: EGPA, HES, CRSsNP and CRSwNP.

30 . The pre-filled syringe according to claim 29 , wherein the pre-filled syringe comprises about 100 mg of the antigen binding protein.

31 . The pre-filled syringe according to claim 29 , wherein the pre-filled syringe comprises about 200 mg of the antigen binding protein.

32 . The pre-filled syringe according to claim 29 , wherein the pre-filled syringe comprises an aqueous liquid formulation at about pH 6.0 containing the antigen binding protein and histidine, trehalose, arginine, EDTA and/or polysorbate 80.

33 . The pre-filled syringe according to claim 29 , for use in the treatment of an IL-5 mediated disease, such as EGPA, HES, CRSsNP and CRSwNP.

34 . The pre-filled syringe according to claim 29 , wherein the pre-filled syringe is provided in a safety syringe device (SSD) or an autoinjector.

Assignments (7)
CHANGE OF ADDRESS Recorded Oct 8, 2025
From: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
Reel/Frame 073032/0390 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2024
From: GLAXOSMITHKLINE SERVICES UNLIMITED
To: GLAXOSMITHKLINE RESEARCH AND DEVELOPMENT LIMITED
Reel/Frame 067713/0829 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2024
From: GLAXOSMITHKLINE RESEARCH AND DEVELOPMENT LIMITED
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
Reel/Frame 067713/0948 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2024
From: AUSTIN, DAREN J.; BERGES, ALIENOR C.; BIRD, NICHOLAS P.; POULIQUEN, ISABELLE J.; ZECCHIN, CHIARA
To: GLAXOSMITHKLINE SERVICES UNLIMITED
Reel/Frame 067713/0705 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2024
From: GLAXOSMITHKLINE LLC
To: GLAXOSMITHKLINE RESEARCH AND DEVELOPMENT LIMITED
Reel/Frame 067714/0270 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2024
From: GLAXOSMITHKLINE RESEARCH AND DEVELOPMENT LIMITED
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
Reel/Frame 067714/0370 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2024
From: MONCK, MYRNA A.; SHUMAN, MELISSA ANN
To: GLAXOSMITHKLINE LLC
Reel/Frame 067714/0150 →