IP Library Patent Application 18201620
Patent Application
App. No. 18/201,620

USE OF ANTI-IL-27 ANTIBODIES

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Quick Facts
Patent No.
US None
App. No.
18/201,620
Abstract

The present disclosure relates to methods of treating cancer comprising administering to a subject an anti-IL-27 antibody and pembrolizumab.

Claims (32)

1 . A method of stimulating an immune response in a subject, the method comprising administering to the subject (i) an antibody that binds human IL-27 or an antigen binding portion thereof (“an anti-IL-27 antibody”), and (ii) pembrolizumab; wherein the anti-IL-27 antibody comprises a heavy chain CDR1 comprising the amino acid sequence set forth in SEQ ID NO: 5, a heavy chain CDR2 comprising the amino acid sequence set forth in SEQ ID NO: 6, a heavy chain CDR3 comprising the amino acid sequence set forth in SEQ ID NO: 7, a light chain CDR1 comprising the amino acid sequence set forth in SEQ ID NO: 13, a light chain CDR2 comprising the amino acid sequence set forth in SEQ ID NO: 14, and a light chain CDR3 comprising the amino acid sequence set forth in SEQ ID NO: 15.

2 . A method of treating a cancer in a subject in need thereof comprising administering to the subject (i) an antibody that binds human IL-27 or an antigen binding portion thereof (“an anti-IL-27 antibody”), and (ii) pembrolizumab; wherein the anti-IL-27 antibody comprises a heavy chain CDR1 comprising the amino acid sequence set forth in SEQ ID NO: 5, a heavy chain CDR2 comprising the amino acid sequence set forth in SEQ ID NO: 6, a heavy chain CDR3 comprising the amino acid sequence set forth in SEQ ID NO: 7, a light chain CDR1 comprising the amino acid sequence set forth in SEQ ID NO: 13, a light chain CDR2 comprising the amino acid sequence set forth in SEQ ID NO: 14, and a light chain CDR3 comprising the amino acid sequence set forth in SEQ ID NO: 15.

3 . The method of claim 2 , wherein the anti-IL-27 antibody is administered at a dose of at least about 0.003 mg/kg to at least about 20 mg/kg.

4 . (canceled)

5 . The method of claim 2 , wherein the anti-IL-27 antibody is administered once about every week, once about every two weeks, once about every three weeks, once about every four weeks, once about every 6 weeks, once about every 8 weeks, or once about every 12 weeks.

6 - 18 . (canceled)

19 . The method of claim 2 , wherein pembrolizumab is administered at a dose of at least about 1 mg/kg to at least about 10 mg/kg.

20 . (canceled)

21 . The method of claim 2 , wherein pembrolizumab is administered at a flat dose.

22 . (canceled)

23 . The method of claim 2 , wherein pembrolizumab is administered once about every week, once about every two weeks, once about every three weeks, or once about every four weeks.

24 - 34 . (canceled)

35 . The method of claim 2 , wherein the anti-IL-27 antibody and pembrolizumab are administered on the same day.

36 . The method of claim 2 , wherein the anti-IL-27 antibody and pembrolizumab are administered concurrently.

37 . The method of claim 2 , wherein the anti-IL-27 antibody and pembrolizumab are administered sequentially.

38 . The method of claim 2 , wherein the anti-IL-27 antibody is administered before pembrolizumab.

39 . The method of claim 2 , wherein the anti-IL-27 antibody is administered after pembrolizumab.

40 . The method of claim 2 , wherein the anti-IL-27 antibody and pembrolizumab are administered on different days.

41 . The method of claim 2 , wherein the anti-IL-27 antibody comprises a heavy chain variable region comprising an amino acid sequence that has at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, [[or]] at least about 99%, or at least 100% sequence identity to the amino acid sequence set forth in SEQ ID NO: 11.

42 . (canceled)

43 . The method of claim 2 , wherein the anti-IL-27 antibody comprises a light chain variable region comprising an amino acid sequence that has at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or at least 100% sequence identity to the amino acid sequence set forth in SEQ ID NO: 19.

44 . (canceled)

45 . (canceled)

46 . The method of claim 2 , wherein the anti-IL-27 antibody comprises a heavy chain comprising the amino acid sequence set forth in SEQ ID NO: 21.

47 . The method of claim 2 , wherein the anti-IL-27 antibody comprises a heavy chain comprising the amino acid sequence set forth in SEQ ID NO: 25.

48 . The method of claim 2 , wherein the anti-IL-27 antibody comprises a light chain comprising the amino acid sequence set forth in SEQ ID NO: 23.

49 . (canceled)

50 . (canceled)

51 . The method of claim 1 , wherein the subject is afflicted with a cancer.

52 - 54 . (canceled)

55 . The method of claim 2 , wherein the subject previously received at least one, at least two, at least three, at least four, or at least five prior anticancer therapies.

56 - 118 . (canceled)

Assignments (1)
SECURITY INTEREST Recorded May 8, 2024
From: COHERUS BIOSCIENCES, INC.; COHERUS INTERMEDIATE CORP.; INTEKRIN THERAPEUTICS INC.; SURFACE ONCOLOGY, LLC; COHERUS ONCOLOGY SUPPORTIVE CARE LLC
To: ANKURA TRUST COMPANY, LLC
Reel/Frame 067348/0160 →