IP Library Granted Patent US 11,142,588
Granted Patent B2
US 11,142,588 · App. 16/719,125 · Granted Oct 12, 2021

Polypeptides which bind C-X-C chemokine receptor type 4 (CXCR4) and methods of treating or reducing the risk of fibrosis and cancer

Inventors: Michael Foley (Coburg, AU); Andrew Pow (Burlingame, CA); Katherine Griffiths (Eltham North, AU); Samantha Cobb (South Yarra, AU); Katerina Viduka (Greensborough, AU)
Assignee: ADALTA LIMITED
C07K17/02A61K38/2228C07K16/18C07K16/2866G01N33/56988G01N33/574A61K2039/505C07K2317/31C07K2317/34C07K2317/56C07K2317/569C07K2317/76C07K2317/92G01N2333/521G01N2800/285G01N2800/323
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Quick Facts
Patent No.
US 11,142,588
App. No.
16/719,125
Granted
Oct 12, 2021
Kind
B2
Abstract

The present disclosure relates to polypeptides (also referred to herein as CXCR4 binding molecules or polypeptides) that are directed against the G-coupled protein receptor CXCR4, also known as Fusin or CD184. The invention also relates to nucleic acids encoding such polypeptides; to methods for preparing such polypeptide; to compositions, and in particular to pharmaceutical compositions that comprise such polypeptides and to uses of such polypeptides for therapeutic or diagnostic purposes.

Claims (24)

1. A polypeptide which binds to human C-X-C chemokine receptor type 4 (CXCR4) comprising:

a scaffold region and first and second binding loop regions contained therein, wherein the scaffold region comprises a sequence which has at least 80% identity to the scaffold region defined by amino acids 1 to 26, 33 to 79 and 88 to 97 of SEQ ID NO:1, and wherein the first binding loop region comprises the sequence of SEQ ID NO:41 and the second binding loop region comprises the sequence of SEQ ID NO:42.

2. A polypeptide comprising a sequence having at least 95% identity to SEQ ID NO:40.

3. The polypeptide according to claim 1 , which is an antagonist of human CXCR4.

4. A conjugate comprising the polypeptide according to claim 1 and an agent.

5. The conjugate according to claim 4 , wherein the agent is selected from a therapeutic agent, a cytotoxin, a detectable label or an agent which extends the half-life of the polypeptide.

6. The conjugate according to claim 5 , wherein the agent which extends the half-life of the polypeptide is an Fc portion of an immunoglobulin.

7. A pharmaceutical composition comprising:

the polypeptide according to claim 1 ; or

a conjugate comprising the polypeptide and an agent.

8. The polypeptide according to claim 1 which inhibits one or more of the following activities:

(i) cAMP in cells expressing CXCR4;

(ii) β-arrestin signalling in cells expressing CXCR4;

(iii) cell proliferation of cells expressing CXCR4;

(iv) metastasis of cells expressing CXCR4;

(v) CXCR4-induced angiogenesis; and/or

(vi) migration of cells expressing CXCR4.

9. The polypeptide according to claim 1 which is in monomeric, dimeric or multimeric form.

10. The polypeptide according to claim 1 which is a heterodimer.

11. A method of treating or reducing the risk of developing fibrosis or cancer in a subject comprising administering to the subject:

the polypeptide according to claim 1 ; or

a conjugate comprising the polypeptide and an agent; or

a pharmaceutical composition comprising the polypeptide or the conjugate.

12. The method according to claim 11 , wherein the fibrosis is idiopathic pulmonary fibrosis.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 23, 2020
From: FOLEY, MICHAEL; POW, ANDREW; GRIFFITHS, KATHERINE; COBB, SAMANTHA; VIDUKA, KATERINA
To: ADALTA PTY LTD
Reel/Frame 052471/0482 →
CHANGE OF NAME Recorded Apr 23, 2020
From: ADALTA PTY LTD
To: ADALTA LIMITED
Reel/Frame 052472/0478 →
Priority Claims (1)
AU 2015900054 · Jan 9, 2015 · national
Continuity (2)
Continuation 15542060
Related Publication 20200231708A1 · Jul 23, 2020