US2021032359A1PendingUtilityA1

Antibodies against phosphorylcholine in combination therapy with biologic agents

Assignee: ATHERA BIOTECHNOLOGIES ABPriority: Mar 4, 2010Filed: Aug 11, 2020Published: Feb 4, 2021
Est. expiryMar 4, 2030(~3.6 yrs left)· nominal 20-yr term from priority
A61P 17/00A61P 37/04A61P 9/00A61P 17/06A61P 29/00A61P 37/06C07K 2317/24C07K 2319/30A61P 3/10A61P 1/00C07K 16/18A61P 13/12A61K 39/39533A61P 19/02C07K 2317/21A61P 9/10A61K 2039/505C07K 16/2887C07K 16/241A61P 25/00A61P 21/04A61P 25/28A61K 35/28A61P 21/00C07K 14/525A61P 35/00
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Claims

Abstract

Antibodies against PC, PC conjugate or bioactive components and/or fragments thereof for use in combination therapy with one or more biologic agents and/or stem cells are disclosed, as well as compositions comprising the antibodies in combination with one or more biologic agents and/or stem cells. Also disclosed are PC conjugates, PC or bioactive components and/or parts/fragments thereof for use in activation immunotherapy prior to or in combination with treatment with biologic agents and/or stem cells for curing, treating, preventing, and/or reducing the risk of developing auto-immune diseases, chronic inflammatory diseases, and cancer diseases, as well as compositions comprising them in combination with biologic agents and/or stem cells.

Claims

exact text as granted — not AI-modified
1 . A method for increasing the efficacy of rituximab in a non-responder mammal to rituximab for curing, treating, preventing, and/or reducing the risk of developing rheumatoid arthritis, said method comprising:
 identifying an individual that is a non-responder to rituximab; and   administering rituximab in combination with antibodies or derivatives thereof against PC or PC conjugate thereof to the non-responder,   wherein said antibodies or derivatives thereof against PC or PC conjugate is selected from the group comprising a monoclonal, polyclonal or chimeric antibody of isotype IgA, IgD, IgE, IgG, IgM, optionally in combination with any suitable excipients or adjuvants; and   wherein said mammal is selected from the group comprising rabbits, dogs, cats, horses and humans.   
     
     
         2 . The method of  claim 1 , wherein administering the rituximab comprises co-administering rituximab simultaneously with the antibodies or derivatives thereof against PC or PC conjugate thereof.

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