Methods for treating chronic spontaneous urticaria by administering an il-4r antagonist
AssigneesSanofi Biotechnology, Regeneron Pharmaceuticals, Inc.
InventorsNikhil Amin, Elizabeth Laws, Leda Mannent, Allen Radin, Aleksandra Stjepanovic, Naimish Patel, Heribert Staudinger
Life of this patent
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Abstract
Methods for treating or preventing chronic spontaneous urticaria in a subject are provided. Methods comprising administering to a subject in need thereof a therapeutic composition comprising an interleukin-4 receptor (IL-4R) antagonist, such as an anti-IL-4R antibody or antigen-binding fragment thereof, are provided.
Claims38
A method for treating a subject having chronic spontaneous urticaria (CSU) comprising administering to the subject an antibody or an antigen-binding fragment thereof that specifically binds interleukin-4 receptor (IL-4R),
- wherein the antibody or antigen-binding fragment thereof comprises three heavy chain CDR sequences comprising SEQ ID NOs:
- 3, 4, and 5, respectively, and three light chain CDR sequences comprising SEQ ID NOs:
- 6, 7, and 8, respectively, and
- wherein the subject was previously ineffectively treated with H1 antihistamine therapy and anti-IgE antibody therapy.
3-5. (canceled)
7-27. (canceled)
A method for treating a subject having chronic spontaneous urticaria (CSU) comprising administering to the subject an antibody or an antigen-binding fragment thereof that specifically binds interleukin-4 receptor (IL-4R),
- wherein the antibody or antigen-binding fragment thereof comprises three heavy chain CDR sequences comprising SEQ ID NOs:
- 3, 4, and 5, respectively, and three light chain CDR sequences comprising SEQ ID NOs:
- 6, 7, and 8, respectively,
- wherein the subject is 12 years old to less than 18 years old,
- wherein the antibody or antigen-binding fragment thereof is administered to the subject as an initial dose followed by one or more secondary doses, and
- wherein the antibody or antigen-binding fragment thereof is administered to the subject in a weight-dependent dosage;
- or
- a method for treating a subject having chronic spontaneous urticaria (CSU) comprising administering to the subject an antibody or an antigen-binding fragment thereof that specifically binds interleukin-4 receptor (IL-4R),
- wherein the antibody or antigen-binding fragment thereof comprises three heavy chain CDR sequences comprising SEQ ID NOs:
- 3, 4, and 5, respectively, and three light chain CDR sequences comprising SEQ ID NOs:
- 6, 7, and 8, respectively,
- wherein the subject is 6 years old to less than 12 years old,
- wherein the antibody or antigen-binding fragment thereof is administered to the subject as an initial dose followed by one or more secondary doses, and
- wherein the antibody or antigen-binding fragment thereof is administered to the subject in a weight-dependent dosage;
- or
- a method for treating a subject having chronic spontaneous urticaria (CSU) comprising administering to the subject an antibody or an antigen-binding fragment thereof that specifically binds interleukin-4 receptor (IL-4R),
- wherein the antibody or antigen-binding fragment thereof comprises three heavy chain CDR sequences comprising SEQ ID NOs:
- 3, 4, and 5, respectively, and three light chain CDR sequences comprising SEQ ID NOs:
- 6, 7, and 8, respectively,
- wherein the subject is 2 years old to less than 6 years old,
- wherein the antibody or antigen-binding fragment thereof is administered to the subject as an initial dose followed by one or more secondary doses, and
- wherein the antibody or antigen-binding fragment thereof is administered to the subject in a weight-dependent dosage.
30-36. (canceled)
A method for treating a subject having chronic spontaneous urticaria (CSU) comprising administering to the subject an antibody or an antigen-binding fragment thereof that specifically binds interleukin-4 receptor (IL-4R),
- wherein the antibody or antigen-binding fragment thereof comprises three heavy chain CDR sequences comprising SEQ ID NOs:
- 3, 4, and 5, respectively, and three light chain CDR sequences comprising SEQ ID NOs:
- 6, 7, and 8, respectively,
- wherein the subject is the subject is 12 years old to less than 18 years old,
- wherein the antibody or antigen-binding fragment thereof is administered to the subject as an initial dose followed by one or more secondary doses,
- wherein the antibody or antigen-binding fragment thereof is administered to the subject in a weight dependent dosage, and
- wherein the subject was previously ineffectively treated with antihistamine therapy or anti-IgE antibody therapy, or
- a method for treating a subject having chronic spontaneous urticaria (CSU) comprising administering to the subject an antibody or an antigen-binding fragment thereof that specifically binds interleukin-4 receptor (IL-4R),
- wherein the antibody or antigen-binding fragment thereof comprises three heavy chain CDR sequences comprising SEQ ID NOs:
- 3, 4, and 5, respectively, and three light chain CDR sequences comprising SEQ ID NOs:
- 6, 7, and 8, respectively,
- wherein the subject is the subject is 6 years old to less than 12 years old,
- wherein the antibody or antigen-binding fragment thereof is administered to the subject as an initial dose followed by one or more secondary doses,
- wherein the antibody or antigen-binding fragment thereof is administered to the subject in a weight dependent dosage, and
- wherein the subject was previously ineffectively treated with antihistamine therapy or anti-IgE antibody therapy;
- or
- a method for treating a subject having chronic spontaneous urticaria (CSU) comprising administering to the subject an antibody or an antigen-binding fragment thereof that specifically binds interleukin-4 receptor (IL-4R),
- wherein the antibody or antigen-binding fragment thereof comprises three heavy chain CDR sequences comprising SEQ ID NOs:
- 3, 4, and 5, respectively, and three light chain CDR sequences comprising SEQ ID NOs:
- 6, 7, and 8, respectively,
- wherein the subject is 2 years old to less than 6 years old,
- wherein the antibody or antigen-binding fragment thereof is administered to the subject as an initial dose followed by one or more secondary doses,
- wherein the antibody or antigen-binding fragment thereof is administered to the subject in a weight dependent dosage, and
- wherein the subject was previously ineffectively treated with antihistamine therapy or anti-IgE antibody therapy.
40-42. (canceled)
44-46. (canceled)
48-58. (canceled)
60-72. (canceled)
75-90. (canceled)
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94-97. (canceled)
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108-117. (canceled)
119-131. (canceled)
Dependencies are inferred from the claim text.