US2017204196A1PendingUtilityA1
Anti-nme antibody
Assignee: MINERVA BIOTECHNOLOGIES CORPPriority: Apr 7, 2014Filed: Apr 7, 2015Published: Jul 20, 2017
Est. expiryApr 7, 2034(~7.7 yrs left)· nominal 20-yr term from priority
A61P 37/04A61P 43/00A61P 35/04A61P 35/00C12N 2800/22C07K 2319/00C07K 16/3092C07K 16/32A61K 39/395C07K 14/7051C12N 5/0693C07K 16/30A61K 2039/505C07K 2317/622A61K 48/00C07K 16/40C12Q 1/6883C07K 2317/73C07K 2317/33C07K 2317/76A61K 39/0011G01N 33/575
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Claims
Abstract
The present application discloses anti-NME antibodies and their use in treating or preventing diseases.
Claims
exact text as granted — not AI-modified1 . A method of treating or preventing cancer in a subject, comprising administering to the subject an antibody made against a member of the NME family.
2 . The method according to claim 1 , wherein the NME family is NME7 family.
3 . The method according to claim 2 , wherein the antibody binds to NME7.
4 . The method according to claim 2 , wherein the antibody binds to NME7-AB or NME-AB-like protein.
5 . The method according to claim 2 , wherein the antibody binds to NME7-X1.
6 . The method according to claim 1 , wherein the antibody inhibits binding between NME7 and its cognate binding partner.
7 . The method according to claim 6 , wherein the cognate binding partner is MUC1*.
8 . The method according to claim 6 , wherein the cognate binding partner is PSMGFR portion of the MUC1* extracellular domain.
9 . The method according to claim 1 , wherein the antibody is generated or selected for its ability to bind to a peptide selected from those listed in FIGS. 16-19 (SEQ ID NOS:88 to 145).
10 . The method according to claim 9 , wherein the peptide is selected from those listed in FIG. 19 (SEQ ID NOS:141 to 145).
11 . The method according to claim 9 , wherein the peptide comprises a peptide, which is highly homologous to, or to which is added or subtracted up to 7 amino acid residues at the N-terminus or C-terminus, of the peptides listed in FIGS. 16-19 (SEQ ID NOS:88 to 145).
12 . The method according to claim 1 , wherein the antibody is selected for its ability to bind to NME7-AB or NME7-X1 but not to NME1.
13 . The method according to claim 1 , wherein the antibody is polyclonal, monoclonal, bivalent, monovalent, bispecific, an antibody fragment containing the variable region, or an antibody mimic.
14 . The method according to claim 1 , wherein the antibody is human or humanized.
15 . The method according to claim 1 , wherein the antibody is a single chain scFv.
16 .- 24 . (canceled)
25 . A chimeric antigen receptor (CAR), for the treatment or prevention of cancer wherein the targeting extracellular portion of the CAR comprises at least a peptide fragment of a member of the NME family.
26 . The chimeric antigen receptor according to claim 25 , wherein the NME family is NME7 family.
27 . The chimeric antigen receptor according to claim 26 , wherein the member of the NME7 family is NME7.
28 . The chimeric antigen receptor according to claim 26 , wherein the member of the NME7 family is NME7-AB or NME-AB-like protein.
29 . The chimeric antigen receptor according to claim 26 , wherein the member of the NME7 family is NME7-X1.
30 .- 78 . (canceled)Join the waitlist — get patent alerts
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