US2020247895A1PendingUtilityA1
Osteoarthritis treatment
Est. expiryDec 22, 2028(~2.4 yrs left)· nominal 20-yr term from priority
A61P 29/00A61K 39/395C07K 16/2866A61K 2039/505C07K 16/243C07K 2317/76C07K 2317/24A61P 19/00A61P 19/02C07K 2317/565A61P 43/00
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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 . A method for decreasing or preventing cartilage damage, osteophyte formation and joint deformation in a human subject with osteoarthritis, comprising the step of administering to the subject an effective amount of an antibody specific for GM-CSF or the GM-CSF Receptor.
2 . The method according to claim 1 , wherein the antibody comprises the heavy chain variable region amino acid sequence of SEQ ID NO: 3, or the light chain variable region amino acid sequence of SEQ ID NO: 4.
3 . The method according to claim 1 , wherein the antibody comprises a H-CDR3 sequence selected from any one of SEQ ID NOs: 5-16, a H-CDR1 sequence of SEQ ID NO: 17, a H-CDR2 sequence of SEQ ID NO: 18, a L-CDR1 sequence of SEQ ID NO: 19, a L-CDR2 sequence of SEQ ID NO: 20 and a L-CDR3 sequence of SEQ ID NO: 21.
4 . The method according to claim 1 , wherein the antibody comprises a H-CDR3 sequence selected from any one of SEQ ID NOs: 28-46.Cited by (0)
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