Compositions and Methods to Regulate Renalase in the Treatment of Cancer

US2021024652A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2021024652-A1
Application numberUS-202016847964-A
CountryUS
Kind codeA1
Filing dateApr 14, 2020
Priority dateJun 26, 2014
Publication dateJan 28, 2021
Grant date

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The invention provides compositions and methods for binding and inhibiting renalase. In one embodiment, the renalase binding molecule inhibits renalase activity. Thus, in diseases and conditions where a reduction of renalase activity is beneficial, such inhibitory renalase binding molecules act as therapeutics.

First claim

Opening claim text (preview).

1 - 36 . (canceled) 37 . A composition comprising an isolated monoclonal antibody, wherein the antibody comprises: a) the heavy chain CDR1 sequence of SEQ ID NO:19; b) the heavy chain CDR2 sequence of SEQ ID NO:20; c) the heavy chain CDR3 sequence of SEQ ID NO:21; d) the light chain CDR1 sequence of SEQ ID NO:22; e) the light chain CDR2 sequence of SEQ ID NO:23; and f) the light chain CDR3 sequence of SEQ ID NO:24. 38 . The composition of claim 37 , wherein the antibody specifically binds to renalase with an affinity of at least 10′ M. 39 . The composition of claim 37 , wherein the antibody specifically binds a peptide sequence as set forth in SEQ ID NO:4. 40 . The composition of claim 37 , wherein the antibody is selected from the group consisting of an immunoconjugate, a defucosylated antibody, and a bispecific antibody. 41 . The composition of claim 40 , wherein the immunoconjugate comprises a therapeutic agent or a detection moiety. 42 . The composition of claim 37 , wherein the antibody is selected from the group consisting of a humanized antibody, a chimeric antibody, a fully human antibody, and an antibody mimetic. 43 . The composition of claim 37 , wherein the antibody comprises a heavy chain sequence as set forth in SEQ ID NO:17. 44 . The composition of claim 37 , wherein the antibody comprises a light chain sequence as set forth in SEQ ID NO:18. 45 . A method of treating or preventing a disease or disorder associated with renalase in a subject, the method comprising the step of administering to the subject the composition of claim 37 . 46 . The method of claim 45 , wherein the composition is administered to the subject in combination with a second therapeutic agent. 47 . The method of claim 45 , wherein the disease or disorder associated with renalase is selected from the group consisting of renal disease, cardiovascular disease, cancer, and any combination thereof 48 . The method of claim 47 , wherein the disease or disorder is cancer, and the cancer is pancreatic cancer or melanoma.

Assignees

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Classifications

  • acting on NADH or NADPH (1.6), e.g. those with a heme protein as acceptor (1.6.2) (general), Cytochrome-b5 reductase (1.6.2.2) or NADPH-cytochrome P450 reductase (1.6.2.4) · CPC title

  • Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation · CPC title

  • Antineoplastic agents · CPC title

  • Complementarity determining region [CDR] · CPC title

  • Complete heavy chain or Fd fragment, i.e. VH + CH1 · CPC title

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Frequently asked questions

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What does patent US2021024652A1 cover?
The invention provides compositions and methods for binding and inhibiting renalase. In one embodiment, the renalase binding molecule inhibits renalase activity. Thus, in diseases and conditions where a reduction of renalase activity is beneficial, such inhibitory renalase binding molecules act as therapeutics.
Who is the assignee on this patent?
Univ Yale
What technology area does this patent fall under?
Primary CPC classification C07K16/40. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Jan 28 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).