US2016185868A1PendingUtilityA1
Osteoarthritis treatment
Est. expiryDec 22, 2028(~2.4 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 29/00A61P 19/00A61P 19/02A61K 39/395A61K 2039/505C07K 2317/24C07K 16/2866C07K 2317/76C07K 2317/565C07K 16/243
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Claims
Abstract
The present invention relates generally to a method for the treatment and/or prophylaxis of osteoarthritis (OA). In accordance with the present invention, an antagonist of GM-CSF can be effective in the treatment of osteoarthritis. An antagonist of GM-CSF includes, but is not limited to, an antibody that is specific for GM-CSF or the GM-CSF receptor. The present invention further provides transgenic animals, such as a GM-CSF knock-out mouse, useful for testing antagonists in certain disease models.
Claims
exact text as granted — not AI-modified1 - 5 . (canceled)
6 . A method for the treatment of osteoarthritis in a human subject, comprising the step of administering to the subject an effective amount of an antibody specific for the GM-CSF receptor.
7 . The method of claim 6 , wherein the antibody comprises an amino acid sequence at least 90% homologous to an amino acid sequence selected from the group consisting of the H-CDR3 sequences of SEQ ID NOs: 28-46.
8 . The method of claim 6 , wherein the antibody comprises an amino acid sequence at least 95% homologous to an amino acid sequence selected from the group consisting of the H-CDR3 sequences of SEQ ID NOs: 28-46.
9 . The method of claim 6 , wherein the antibody comprises an amino acid sequence selected from the group consisting of the H-CDR3 sequences of SEQ ID NOs: 28-46.
10 . The method of claim 6 , wherein the antibody comprises an H-CDR3 amino acid sequence of SEQ ID NO: 32.
11 . The method of claim 6 , wherein the antibody is a chimeric, humanised or human antibody.
12 . The method of claim 11 , wherein the antibody is a humanised antibody.
13 . The method of claim 6 , wherein the antibody further comprises one or more pharmaceutically acceptable carriers or diluents.Cited by (0)
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