US2017275368A1PendingUtilityA1
Antibodies against human csf-1r and uses thereof
Est. expiryMar 5, 2030(~3.6 yrs left)· nominal 20-yr term from priority
A61P 37/00A61P 35/00A61P 35/02A61P 35/04A61P 29/00A61P 19/08A61P 19/10C07K 16/2866C07K 2317/76C07K 2317/92C07K 2317/73C07K 16/28A61K 39/395C12N 15/11
53
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Claims
Abstract
The present invention relates to antibodies against human CSF-1R (CSF-1R antibody), methods for their production, pharmaceutical compositions containing said antibodies, and uses thereof.
Claims
exact text as granted — not AI-modified1 - 16 . (canceled)
17 . A method for treating a patient suffering from cancer associated with macrophage colony-stimulating factor 1 receptor (CSF-1R) expression, the method comprising administering to the patient an effective amount of an isolated antibody binding to human CSF-1R, or an antibody fragment thereof,
wherein the antibody comprises a heavy chain variable domain comprising a CDR3 region of SEQ ID NO: 1, a CDR2 region of SEQ ID NO: 2, and a CDR1 region of SEQ ID NO:3, and a light chain variable domain comprising a CDR3 region of SEQ ID NO: 4, a CDR2 region of SEQ ID NO:5, and a CDR1 region of SEQ ID NO:6.
18 . A method for treating a patient suffering from bone loss associated with CSF-1R expression, the method comprising administering to the patient an effective amount of an isolated antibody binding to human CSF-1R, or an antibody fragment thereof,
wherein the antibody comprises a heavy chain variable domain comprising a CDR3 region of SEQ ID NO: 1, a CDR2 region of SEQ ID NO: 2, and a CDR1 region of SEQ ID NO:3, and a light chain variable domain comprising a CDR3 region of SEQ ID NO: 4, a CDR2 region of SEQ ID NO:5, and a CDR1 region of SEQ ID NO:6.
19 . A method for treating a patient suffering from metastasis associated with CSF-1R expression, the method comprising administering to the patient an effective amount of an isolated antibody binding to human CSF-1R, or an antibody fragment thereof,
wherein the antibody comprises a heavy chain variable domain comprising a CDR3 region of SEQ ID NO: 1, a CDR2 region of SEQ ID NO: 2, and a CDR1 region of SEQ ID NO:3, and a light chain variable domain comprising a CDR3 region of SEQ ID NO: 4, a CDR2 region of SEQ ID NO:5, and a CDR1 region of SEQ ID NO:6.
20 . A method for treating a patient suffering from inflammatory diseases associated with CSF-1R expression, the method comprising administering to the patient an effective amount of an isolated antibody binding to human CSF-1R, or an antibody fragment thereof,
wherein the antibody comprises a heavy chain variable domain comprising a CDR3 region of SEQ ID NO: 1, a CDR2 region of SEQ ID NO: 2, and a CDR1 region of SEQ ID NO:3, and a light chain variable domain comprising a CDR3 region of SEQ ID NO: 4, a CDR2 region of SEQ ID NO:5, and a CDR1 region of SEQ ID NO:6.
21 . The method of claim 17 , wherein the antibody, or antibody fragment thereof, of claim 1 , wherein the antibody comprises a heavy chain variable domain comprising the amino acid sequence of SEQ ID NO: 7, and a light chain variable domain comprising the amino acid sequence of SEQ ID NO:8.
22 . The method of claim 17 , wherein the antibody, or antibody fragment thereof, is capable of binding human CSF-1R with a Kd value of 1 nM or lower.
23 . The method of claim 17 , wherein the antibody, or antibody fragment thereof, inhibits human CSF-1 binding to CSF-1R with an IC50 value of 25 ng/ml or lower.
24 . The method of claim 17 , wherein the antibody, or antibody fragment thereof, is human IgG1 subclass or is of human IgG4 subclass.
25 . The method of claim 17 , wherein the antibody, or antibody fragment thereof, is a CDR grafted, humanized, T cell epitope depleted, chimeric, single chain, or multispecific antibody
26 . The method of claim 17 , wherein the antibody, or antibody fragment thereof, is a monoclonal antibody.
27 . The method of claim 17 , wherein the antibody, or antibody fragment thereof, is conjugated to a cytotoxic agent.
28 . The method of claim 27 , wherein the cytotoxic agent is a chemotherapeutic agent, a growth inhibitory agent, a toxin, or a radioactive isotope.Join the waitlist — get patent alerts
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