US2007065442A1PendingUtilityA1
Compositions and methods for treating hyperimmune response in the eye
Est. expiryJun 5, 2021(expired)· nominal 20-yr term from priority
C07K 2317/54A61K 2039/505A61K 2039/54A61K 39/3955C07K 2317/73A61P 27/02A61K 2039/545A61K 45/06C07K 16/24C07K 2317/76C07K 16/249
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Claims
Abstract
The present invention comprises and utilizes methods and compositions for treating hyperimmune reactions in the eye. Compositions comprising antibodies to gamma interferon alone and in combination with other drugs are described. Also disclosed in the invention are methods of applying a composition comprising interferon gamma antibodies topically to the eye to treat hyperimmune reactions, such as transplant rejection, uveitis, autoimmune diseases of the eye, and ocular disorders incidental to or connected with autoimmune diseases.
Claims
exact text as granted — not AI-modified1 - 5 . (canceled)
6 . A method of treating uveitis in a patient, said method comprising administering to the patient a combination of an effective amount of an antibody to gamma interferon and an effective amount of a chemotherapeutic agent.
7 . The method of claim 6 , wherein said antibody is selected from the group consisting of a polyclonal antibody, a monoclonal antibody, a humanized antibody, a synthetic antibody, a heavy chain antibody, a biologically active fragment of an antibody, wherein the biologically active fragment comprises an Fv fragment, an Fab fragment or an F(ab) 2 fragment, and combinations thereof.
8 . The method of claim 6 , wherein said antibody is administered by the route selected from the group consisting of intramuscularly, intravenously, intradermally, cutaneously, ionophoretically, topically, and locally.
9 . The method of claim 8 , wherein the antibody is administered topically.
10 . The method of claim 9 , wherein the antibody is selected from the group consisting of a polyclonal antibody, a monoclonal antibody, a humanized antibody, a synthetic antibody, a heavy chain antibody, a biologically active fragment of an antibody, wherein the biologically active fragment comprises an Fv fragment, an Fab fragment or an F(ab) 2 fragment, and combinations thereof.
11 . The method of claim 10 , wherein the heavy chain antibody is selected from the group consisting of a camelid antibody, a heavy chain disease antibody, and a variable heavy chain immunoglobulin.Join the waitlist — get patent alerts
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