US2020222463A1PendingUtilityA1

Pharmaceutical Composition for Cancer Treatment

Assignee: SHIONOGI & COPriority: Mar 29, 2017Filed: Jan 2, 2020Published: Jul 16, 2020
Est. expiryMar 29, 2037(~10.7 yrs left)· nominal 20-yr term from priority
A61K 35/17C07K 2317/76C07K 2317/732C07K 16/2866C07K 16/2827C07K 16/2818A61K 2039/507A61P 35/00A61K 2039/505A61K 47/6435A61K 47/6883A61K 9/0019G01N 33/5011A61K 47/60A61K 2039/572A61K 39/39533
64
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

The disclosure provides a pharmaceutical composition with a polypeptide that binds to a peptide produced by cDNA of GenBank ACC No. NM_005201.3 or NM_007720.2, and methods of use thereof.

Claims

exact text as granted — not AI-modified
1 . A method of treating cancer in a subject in need thereof, comprising
 administering to the subject a therapeutically effective amount of a pharmaceutical composition comprising an antibody against CCR8.   
     
     
         2 . (canceled) 
     
     
         3 . The method according to  claim 1 , wherein the cancer is breast cancer. 
     
     
         4 . The method according to  claim 1 , wherein the cancer is colorectal cancer. 
     
     
         5 . The method according to  claim 1 , wherein the cancer is kidney cancer. 
     
     
         6 . The method according  claim 1 , wherein the cancer is sarcoma. 
     
     
         7 . The method according to  claim 1 , wherein the cancer is lung cancer. 
     
     
         8 - 10 . (canceled) 
     
     
         11 . The method according to  claim 1 , wherein the antibody is an IgG antibody. 
     
     
         12 . The method according to  claim 1 , wherein the antibody against CCR8 is a CCR8-neutralizing antibody. 
     
     
         13 . The method according to  claim 1 , wherein the therapeutically effective amount is at a dose of 5 mg to 5000 mg. 
     
     
         14 . The method according to  claim 1 , wherein the therapeutically effective amount is at a dose of 10 mg to 500 mg. 
     
     
         15 . The method according to  claim 1 , wherein the antibody is administered intravenously. 
     
     
         16 . The method according to  claim 1 , wherein the antibody is administered intraperitoneally. 
     
     
         17 . The method according to  claim 1 , wherein the antibody has antibody-dependent cell-mediated cytotoxicity (ADCC) activity against cells expressing CCR8. 
     
     
         18 . The method according to  claim 1 , wherein in the administering step, the only antibody administered is the antibody against CCR8. 
     
     
         19 . The method according to  claim 1 , wherein an Fc region of the antibody against CCR8 is free from a fucose bond with N-acetylglucosamine. 
     
     
         20 . The method according to  claim 1 , further comprising administering an anti-PD-1 antibody or an anti-PD-L1 antibody. 
     
     
         21 . The method according to  claim 1 , wherein the method further comprises administering at least one antibody selected from the group consisting of nivolumab, pembrolizumab, atezolizumab, avelumab, and durvalumab.

Join the waitlist — get patent alerts

Track US2020222463A1 — get alerts on status changes and closely related new filings.

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