US2012230997A1PendingUtilityA1
Anti-factor B antibodies and their uses
Assignee: CAMPAGNE MENNO VAN LOOKERENPriority: Nov 8, 2007Filed: Jan 31, 2012Published: Sep 13, 2012
Est. expiryNov 8, 2027(~1.3 yrs left)· nominal 20-yr term from priority
A61P 27/02C07K 16/40C07K 2317/56C07K 2317/76
48
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Claims
Abstract
The invention concerns the prevention and treatment of complement-associated eye conditions, such as choroidal neovascularization (CNV) and age-related macular degeneration (AMD), by administration of factor B antagonists.
Claims
exact text as granted — not AI-modified1 . A method for the prevention or treatment of a complement-associated eye condition comprising administering to a subject in need an effective amount of a factor B antagonist.
2 . The method of claim 1 , wherein said subject is a mammal.
3 . The method of claim 2 , wherein said subject is a human.
4 . The method of claim 3 , wherein said factor B antagonist is selected from the group consisting of anti-factor B antibodies and fragments thereof, binding polypeptides, peptides, and non-peptide small molecules.
5 . The method of claim 4 , wherein said factor B antagonist is an antibody or an antibody fragment.
6 . The method of claim 5 , wherein said antibody or antibody fragment binds essentially to the same epitope as anti-factor B antibody 1F7.
7 . The method of claim 5 , wherein said antibody or antibody fragment comprises the light and/or heavy chain hypervariable region sequences of anti-factor B antibody 1F7 (SEQ ID NOs: 1 and 2, respectively).
8 . The method of claim 5 , wherein said antibody or antibody fragment comprises the light and/or heavy chain variable region sequence of anti-factor antibody 1F7 (SEQ ID NOs: 1 and 2, respectively).
9 . The method of claim 5 , which is antibody 1F7 comprising a light chain sequence of SEQ ID NO: 1 and the heavy chain sequence of SEQ ID NO: 2.
10 . The method of claim 5 , wherein said antibody or antibody fragment binds to the active site of factor B.
11 . The method of claim 5 , wherein said antibody or antibody fragment binds to an epitope including active site residues of factor B.
12 . The method of claim 5 , wherein said antibody fragment is selected from the group consisting of Fab, Fab′, F(ab′) 2 , scFv, (scFv) 2 , dAb, complementarity determining region (CDR) fragments, linear antibodies, single-chain antibody molecules, minibodies, diabodies, and multispecific antibodies formed from antibody fragments.
13 . The method of claim 12 , wherein said antibody fragment is a Fab, Fab′, F(ab′) 2 , scFv, or (scFv) 2 fragment.
14 . The method of claim 1 , wherein said complement-associated eye condition is selected from the group consisting of age-related macular degeneration (AMD), choroidal neovascularization (CNV), uveitis, diabetic and other ischemia-related retinopathies, diabetic macular edema, pathological myopia, von Hippel-Lindau disease, histoplasmosis of the eye, Central Retinal Vein Occlusion (CRVO), corneal neovascularization, and retinal neovascularization.
15 . The method of claim 14 , wherein said AMD is dry AMD.
16 . The method of claim 14 , wherein said AMD is wet AMD.Join the waitlist — get patent alerts
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