US2022153851A1PendingUtilityA1

Antibodies that Bind Colony Stimulating Factor 1 Receptor (CSF1R)

Assignee: FIVE PRIME THERAPEUTICS INCPriority: May 4, 2010Filed: Oct 28, 2021Published: May 19, 2022
Est. expiryMay 4, 2030(~3.8 yrs left)· nominal 20-yr term from priority
C07K 2317/76A61P 1/04C07K 2317/92C12N 15/11A61P 19/08C07K 2317/24A61P 1/16C07K 2317/73C07K 16/2866A61P 19/02A61P 37/04A61P 1/00A61K 39/395C07K 14/435A61K 38/18C07K 2317/51C07K 2317/567A61K 39/3955A61P 25/00C12N 15/63A61P 35/00C07K 14/475C07K 2317/33A61K 39/39558A61P 31/14C07K 2317/565A61K 48/00A61P 37/06C07K 2317/55C07K 16/28C07K 2317/52A61P 13/10A61P 13/08A61P 15/00A61P 29/00A61P 7/00C07K 16/22A61P 11/00A61P 35/02C07K 2317/515A61P 31/12C07K 16/24A61P 19/10A61P 37/00A61P 37/02A61K 38/17C07K 16/18A61P 19/00A61P 17/00A61K 45/06A61P 1/18
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Claims

Abstract

Antibodies that bind CSF1R are provided. Antibody heavy chains and light chains that are capable of forming antibodies that bind CSF1R are also provided. Polynucleotides encoding antibodies to CSF1R are provided. Polynucleotides encoding antibody heavy chains and lights chains are also provided. Methods of treatment using antibodies to CSF1R are provided. Such methods include, but are not limited to, methods of treating rheumatoid arthritis, bone loss, and multiple sclerosis.

Claims

exact text as granted — not AI-modified
1 .- 83 . (canceled) 
     
     
         84 . A conjugate comprising a cytotoxic agent and an antibody that binds to human colony stimulating factor 1 receptor (CSF1R); wherein the antibody comprises a heavy chain comprising a heavy chain (HC) CDR1 having the sequence of SEQ ID NO:15, an HC CDR2 having the sequence of SEQ ID NO:16, and an HC CDR3 having the sequence of SEQ ID NO:17, and a light chain comprising a light chain (LC) CDR1 having the sequence of SEQ ID NO:18, a LC CDR2 having the sequence of SEQ ID NO:19, and a LC CDR3 having the sequence of SEQ ID NO:20. 
     
     
         85 . The conjugate of  claim 84 , wherein the cytotoxic agent is a radioisotope, toxin, or chemotherapy agent. 
     
     
         86 . The conjugate of  claim 84 , wherein the cytotoxic agent is a chemotherapy agent. 
     
     
         87 . The conjugate of  claim 84 , wherein the conjugate further comprises a label. 
     
     
         88 . A conjugate comprising a label and an antibody that binds to human colony stimulating factor 1 receptor (CSF1R); wherein the antibody comprises a heavy chain comprising a heavy chain (HC) CDR1 having the sequence of SEQ ID NO:15, an HC CDR2 having the sequence of SEQ ID NO:16, and an HC CDR3 having the sequence of SEQ ID NO:17, and a light chain comprising a light chain (LC) CDR1 having the sequence of SEQ ID NO:18, a LC CDR2 having the sequence of SEQ ID NO:19, and a LC CDR3 having the sequence of SEQ ID NO:20. 
     
     
         89 . The conjugate of  claim 88 , wherein the label facilitates detection of the antibody. 
     
     
         90 . The conjugate of  claim 88 , wherein the label facilitates detection of human CSF1R. 
     
     
         91 . The conjugate of  claim 88 , wherein the label is a radioisotope, fluorescent group, enzymatic group, chemiluminescent group, biotin, epitope tag, or metal-binding tag. 
     
     
         92 . The conjugate of  claim 84 , wherein the antibody blocks binding of human colony stimulating factor 1 (CSF-1) and human interleukin 34 (IL-34) to human CSF1R. 
     
     
         93 . The conjugate of  claim 84 , wherein the antibody heavy chain comprises the amino acid sequence of SEQ ID NO: 39 and wherein the antibody light chain comprises the amino acid sequence of SEQ ID NO: 46. 
     
     
         94 . The conjugate of  claim 84 , wherein the antibody is an antigen binding fragment. 
     
     
         95 . The conjugate of  claim 94 , wherein the antibody is a Fab, an Fv, an scFv, a Fab′, or a (Fab′)2. 
     
     
         96 . The conjugate of  claim 84 , wherein the antibody is an IgG. 
     
     
         97 . The conjugate of  claim 84 , wherein the antibody is an IgG4 comprising an S241P mutation in at least one IgG4 heavy chain constant region. 
     
     
         98 . The conjugate of  claim 84 , wherein the antibody comprises a full length heavy chain and/or a full length light chain. 
     
     
         99 . The conjugate of  claim 93 , wherein the antibody is an antigen binding fragment. 
     
     
         100 . The conjugate of  claim 99 , wherein the antibody is a Fab, an Fv, an scFv, a Fab′, or a (Fab′)2. 
     
     
         101 . The conjugate of  claim 93 , wherein the antibody is an IgG. 
     
     
         102 . The conjugate of  claim 93 , wherein the antibody is an IgG4 comprising an S241P mutation in at least one IgG4 heavy chain constant region. 
     
     
         103 . The conjugate of  claim 93 , wherein the antibody comprises a full length heavy chain and/or a full length light chain. 
     
     
         104 . The conjugate of  claim 84 , wherein the antibody heavy chain comprises the amino acid sequence of SEQ ID NO: 53 and wherein the antibody light chain comprises the amino acid sequence of SEQ ID NO: 60. 
     
     
         105 . A pharmaceutical composition comprising the conjugate of  claim 84  and at least one pharmaceutically acceptable carrier.

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