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
46
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

The present application discloses anti-NME antibodies and their use in treating or preventing diseases.

Claims

exact text as granted — not AI-modified
1 . 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

Track US2017204196A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.