IP Library Granted Patent US 10,167,338
Granted Patent B2
US 10,167,338 · App. 15/229,336 · Granted Jan 1, 2019

Method of treating cancer using IL2R beta/common gamma chain antibodies

Inventors: Cheng-I Wang (Singapore, SG); Peter Brauer (Singapore, SG); Siok Ping Yeo (Singapore, SG); Hwee Ching Tan (Singapore, SG); John Edward Connolly (Singapore, SG)
Assignee: AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH
C07K16/2866A61K39/3955A61K47/6849C07K16/1036C07K16/468A61K38/1709A61K2039/505A61K2039/57C07K2317/31C07K2317/33C07K2317/51C07K2317/515C07K2317/524C07K2317/526C07K2317/565C07K2317/60C07K2317/622C07K2317/64C07K2317/75C07K2317/76C07K2317/92C07K2317/94C07K2319/00
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Quick Facts
Patent No.
US 10,167,338
App. No.
15/229,336
Granted
Jan 1, 2019
Kind
B2
Abstract

Anti-CD122 and/or γc antibodies and fragments thereof are disclosed. Also disclosed are compositions comprising such antibodies and fragments, and uses and methods using the same.

Claims (48)

1. A method of treating cancer in a patient suffering from a cancer comprising administering an effective amount of an antibody or antigen binding fragment thereof to the patient, wherein the antibody or antigen binding fragment thereof comprises:

(a) an antigen binding fragment which binds to CD122, the antigen binding fragment having at least one light chain variable region comprising the following CDRs:

LC-CDR1:

(SEQ ID NO: 2)

TGTSSDIGHYDFVS,

LC-CDR2:

(SEQ ID NO: 3)

DINNRPS, and

LC-CDR3:

(SEQ ID NO: 4)

SAYTSSDTLV,

and having at least one heavy chain variable region comprising the following CDRs:

HC-CDR1:

(SEQ ID NO: 36)

NYYMH,

HC-CDR2:

(SEQ ID NO: 37)

AIMPSRGGTSYPQKFQG, and

HC-CDR3:

(SEQ ID NO: 38)

GEYYYDSSGYYY; and

(b) an antigen binding fragment which binds to common γ chain (γc), the antigen binding fragment having at least one light chain variable region comprising the following CDRs:

LC-CDR1:

(SEQ ID NO: 68)

RSSQSLLHSNGYNYLD,

LC-CDR2:

(SEQ ID NO: 69)

LGSNRDS, and

LC-CDR3:

(SEQ ID NO: 70)

MQGTHWPWT,

and having at least one heavy chain variable region comprising the following CDRs:

HC-CDR1:

(SEQ ID NO: 48)

GYYWS,

HC-CDR2:

(SEQ ID NO: 49)

EINHSGSTNYNPSLKS, and

HC-CDR3:

(SEQ ID NO: 77)

SPGGYSGGYFQH.

2. The method of claim 1 , wherein the antibody or antigen binding fragment thereof comprises:

(i) a first CD122 binding polypeptide, comprising:

(a) a binding unit VL1 consisting of the amino acid sequence of SEQ ID NO:1, and

(b) a binding unit VH1 consisting of the amino acid sequence of SEQ ID NO:35; and

(ii) a second γc binding polypeptide, comprising:

(c) a binding unit VL2 consisting of the amino acid sequence of SEQ ID NO:67, and

(d) a binding unit VH2 consisting of the amino acid sequence of SEQ ID NO:76.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 6, 2016
From: WANG, CHENG-I; BRAUER, PETER; YEO, SIOK PING; TAN, HWEE CHING; CONNOLLY, JOHN EDWARD
To: AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH
Reel/Frame 039635/0831 →
Priority Claims (1)
SG 10201506227V · Aug 6, 2015 · national
Continuity (1)
Related Publication 20160367664A1 · Dec 22, 2016
Cited By (1)
US 12,540,188