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US Patent 10323093 Cancer immunotherapy by disrupting PD-1/PD-L1 signaling

Patent 10323093 was granted and assigned to Bristol-Myers Squibb on June, 2019 by the United States Patent and Trademark Office.

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Is a
Patent
Patent
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Patent attributes

Patent Applicant
Bristol-Myers Squibb
Bristol-Myers Squibb
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Current Assignee
Bristol-Myers Squibb
Bristol-Myers Squibb
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Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
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Patent Number
103230930
Patent Inventor Names
Jon M. Wigginton0
Xi-Tao Wang0
Ashok K. Gupta0
John P. Cogswell0
Maria Jure-Kunkel0
Stacie M. Goldberg0
Date of Patent
June 18, 2019
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Patent Application Number
162306570
Date Filed
December 21, 2018
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Patent Citations
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US Patent 10138299 Cancer immunotherapy by disrupting PD-1/PD-L1 signaling
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US Patent 10072082 Cancer immunotherapy by disrupting PD-1/PD-L1 signaling
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Patent Citations Received
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US Patent 11001630 Human antibodies that bind lymphocyte activation Gene-3 (LAG-3), and uses thereof
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US Patent 11008391 Anti-PD-1 antibodies
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US Patent 11643465 Anti-PD-1 antibodies
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US Patent 11274152 Combination of anti-LAG-3 antibodies and anti-PD-1 antibodies to treat tumors
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US Patent 11299543 Use of an anti-PD-1 antibody in combination with an anti-CD30 antibody in cancer treatment
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US Patent 11767361 Method of treating lung cancer
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US Patent 11345752 Optimization of antibodies that bind lymphocyte activation gene-3 (LAG-3), and uses thereof
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...
Patent Primary Examiner
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Ilia I Ouspenski
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Patent abstract

The disclosure provides a method for immunotherapy of a subject afflicted with cancer, comprises administering to the subject a composition comprising a therapeutically effective amount of an antibody that inhibits signaling from the PD-1/PD-L1 signaling pathway. This disclosure also provides a method for immunotherapy of a subject afflicted with cancer comprising selecting a subject that is a suitable candidate for immunotherapy based on an assessment that the proportion of cells in a test tissue sample from the subject that express PD-L1 on the cell surface exceeds a predetermined threshold level, and administering a therapeutically effective amount of an anti-PD-1 antibody to the selected subject. The invention additionally provides rabbit mAbs that bind specifically to a cell surface-expressed PD-L1 antigen in a FFPE tissue sample, and an automated IHC method for assessing cell surface expression in FFPE tissues using the provided anti-PD-L1 Abs.

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