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公开(公告)号:US12202892B2
公开(公告)日:2025-01-21
申请号:US16839249
申请日:2020-04-03
Applicant: Janssen Biotech, Inc.
Inventor: Marc Chevrier , Jarrat Jordan
IPC: A61K39/395 , A61K47/12 , A61K47/26 , A61P37/02 , C07K16/24 , A61K9/00 , A61K31/4706 , A61K31/519 , A61K31/573 , A61K39/00
Abstract: Methods for administration of an anti-IFN-α/-ω antibody by subcutaneous or intravenous administration in a clinically proven safe amount are provided. Also provided are methods for clinically proven safe treatment of IFN-I mediated diseases, such as systemic lupus erythematosus (SLE), by subcutaneous or intravenous administration of an anti-IFN-α/-ω antibody.
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公开(公告)号:US12009079B2
公开(公告)日:2024-06-11
申请号:US16663527
申请日:2019-10-25
Applicant: Janssen Biotech, Inc.
Inventor: Matteo Cesaroni , Marc Chevrier , Jarrat Jordan , Jessica Schreiter
IPC: C07K14/56 , C12Q1/6809 , G16H20/10 , G16H50/30
CPC classification number: G16H20/10 , C07K14/56 , C12Q1/6809 , G16H50/30 , C07K2317/565 , C12Q2539/00 , C12Q2545/114
Abstract: Type I interferon (IFN-I) signatures are useful in methods of diagnosing whether a subject (or patient) with IFN-I mediated disease will be responsive to treatment with an IFN-I inhibitor and treating or refraining from treating the subjects.
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公开(公告)号:US11197913B2
公开(公告)日:2021-12-14
申请号:US16993556
申请日:2020-08-14
Applicant: Janssen Biotech, Inc.
Inventor: Marc Chevrier , Kamyar Farahi , Newman Yeilding
IPC: A61K39/395 , C07K16/24 , A61K38/20 , A01K67/027 , A61K39/00 , C07K14/54 , A61K35/12
Abstract: A method of treating an IL-12/23-related disease in a patient using an increasing dosing interval, comprises increasing the dosing interval of IL-12/IL-23 antibody to a patient, wherein the antibody is administered initially and after 4 weeks, after 16 weeks and after 28 weeks, and increasing the dosing interval after 28 weeks to an increased interval, e.g., every 16, 20 or 24 weeks.
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公开(公告)号:US10765724B2
公开(公告)日:2020-09-08
申请号:US15471790
申请日:2017-03-28
Applicant: Janssen Biotech, Inc.
Inventor: Marc Chevrier , Kamyar Farahi , Newman Yeilding
IPC: A61K38/20 , A61K39/395 , C07K16/24 , A01K67/027 , A61K39/00 , C07K14/54 , A61K35/12
Abstract: A method of treating an IL-12/23-related disease in a patient using an increasing dosing interval, comprises increasing the dosing interval of IL-12/IL-23 antibody to a patient, wherein the antibody is administered initially and after 4 weeks, after 16 weeks and after 28 weeks, and increasing the dosing interval after 28 weeks to an increased interval, e.g., every 16, 20 or 24 weeks.
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公开(公告)号:US20180036379A1
公开(公告)日:2018-02-08
申请号:US15471790
申请日:2017-03-28
Applicant: Janssen Biotech, Inc.
Inventor: Marc Chevrier , Kamyar Farahi , Newman Yeilding
IPC: A61K38/20 , C07K16/24 , A61K39/00 , A61K39/395 , A01K67/027 , C07K14/54
Abstract: A method of treating an IL-12/23-related disease in a patient using an increasing dosing interval, comprises increasing the dosing interval of IL-12/IL-23 antibody to a patient, wherein the antibody is administered initially and after 4 weeks, after 16 weeks and after 28 weeks, and increasing the dosing interval after 28 weeks to an increased interval, e.g., every 16, 20 or 24 weeks.
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公开(公告)号:US20200317771A1
公开(公告)日:2020-10-08
申请号:US16839249
申请日:2020-04-03
Applicant: Janssen Biotech, Inc.
Inventor: Marc Chevrier , Jarrat Jordan
Abstract: Methods for administration of an anti-IFN-α/-ω antibody by subcutaneous or intravenous administration in a clinically proven safe amount are provided. Also provided are methods for clinically proven safe treatment of IFN-I mediated diseases, such as systemic lupus erythematosus (SLE), by subcutaneous or intravenous administration of an anti-IFN-α/-ω antibody.
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