US2024043546A1PendingUtilityA1
Compositions and methods for treatment of thyroid eye disease
Est. expiryOct 14, 2040(~14.3 yrs left)· nominal 20-yr term from priority
C07K 2317/56A61P 27/02A61P 5/14A61K 2039/545A61K 2039/54A61K 2039/505C07K 16/2863A61K 38/00C07K 16/18A61K 47/6849A61K 47/6803A61K 9/0019C07K 2317/51C07K 2317/515C07K 2317/565C07K 2317/76C07K 2317/94C07K 2317/21C07K 2317/24C07K 2317/92C07K 2317/524C07K 2317/77
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Claims
Abstract
Antibodies and compositions against IGF-1R and uses thereof are provided herein.
Claims
exact text as granted — not AI-modified1 .- 47 . (canceled)
48 . A method of treating thyroid eye disease by inhibiting insulin-like growth factor I receptor (IGF-IR) activity in a subject in need thereof, the method comprising:
administering a first dose of a pharmaceutical composition comprising an antibody at a dose of 10 mg/kg to the subject in need thereof; administering a second dose of the pharmaceutical composition comprising the antibody at a dose of 10 mg/kg to the subject 3 weeks after the first dose; and administering three or more subsequent doses of the pharmaceutical composition comprising the antibody at a dose of 10 mg/kg to the subject every 3 weeks, wherein the antibody comprises a light chain variable region having the amino acid sequence of SEQ ID NO: 13 and a heavy chain variable region having the amino acid sequence of SEQ ID NO: 14.
49 . The method of claim 48 , wherein the subject is administered the pharmaceutical composition for a total of 5 doses to about 8 doses.
50 . The method of claim 49 , wherein the subject is administered the pharmaceutical composition for a total of 5 doses.
51 . The method of claim 49 , wherein the subject is administered the pharmaceutical composition for a total of 8 doses.
52 . The method of claim 48 , wherein the antibody comprises a light chain having the amino acid sequence of SEQ ID NO: 93 and a heavy chain having the amino acid sequence of SEQ ID NO: 92.
53 . The method of claim 49 , wherein the antibody comprises a light chain having the amino acid sequence of SEQ ID NO: 93 and a heavy chain having the amino acid sequence of SEQ ID NO: 92.
54 . The method of claim 50 , wherein the antibody comprises a light chain having the amino acid sequence of SEQ ID NO: 93 and a heavy chain having the amino acid sequence of SEQ ID NO: 92.
55 . The method of claim 51 , wherein the antibody comprises a light chain having the amino acid sequence of SEQ ID NO: 93 and a heavy chain having the amino acid sequence of SEQ ID NO: 92.
56 . The method of claim 48 , wherein the pharmaceutical composition is administered intravenously or subcutaneously.
57 . The method of claim 56 , wherein the pharmaceutical composition is administered intravenously.
58 . The method of claim 56 , wherein the pharmaceutical composition is administered subcutaneously.
59 . The method of claim 48 , wherein treating the thyroid eye disease reduces proptosis in an eye in the subject.
60 . The method of claim 49 , wherein treating the thyroid eye disease reduces proptosis in an eye in the subject.
61 . The method of claim 50 , wherein treating the thyroid eye disease reduces proptosis in an eye in the subject.
62 . The method of claim 51 , wherein treating the thyroid eye disease reduces proptosis in an eye in the subject.
63 . The method of claim 59 , wherein proptosis is reduced by at least 2 mm.
64 . The method of claim 48 , wherein treating the thyroid eye disease reduces clinical activity score (CAS) in the subject.
65 . The method of claim 48 , wherein treating the thyroid eye disease reduces proptosis by at least 2 mm and reduces clinical activity score (CAS) of the subject.
66 . The method of claim 48 , wherein treating the thyroid eye disease improves or reduces the severity of diplopia in the subject.
67 . The method of claim 66 , wherein the diplopia is constant diplopia, inconstant diplopia, or intermittent diplopia.Cited by (0)
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