IP Library Granted Patent US 10,822,381
Granted Patent B2
US 10,822,381 · App. 15/911,017 · Granted Nov 3, 2020

Chlorotoxin variants, conjugates, and methods for their use

Inventor: James M. Olson (Seattle, WA)
Assignee: Fred Hutchinson Cancer Research Center
C07K14/47A61K47/6415C07K14/43522A61K38/00
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Quick Facts
Patent No.
US 10,822,381
App. No.
15/911,017
Granted
Nov 3, 2020
Kind
B2
Abstract

Chlorotoxin variants, chlorotoxin variant conjugates, compositions that include the chlorotoxin variants or conjugates, and methods for using the chlorotoxin variants, conjugates, and compositions.

Claims (19)

1. A method for treating a disease or condition treatable by administering a chlorotoxin conjugate, the method comprising administering an effective amount of the chlorotoxin conjugate comprising a modified chlorotoxin polypeptide covalently conjugated to a fluorescent moiety comprising indocyanine green, the modified chlorotoxin polypeptide comprising an amino acid sequence of native chlorotoxin (SEQ ID NO: 1) in which lysine residue K15, lysine residue K23, or a combination thereof are substituted with an amino acid other than lysine, and wherein the chlorotoxin conjugate binds chlorotoxin binding sites expressed by cancer cells.

2. The method of claim 1 , wherein the modified chlorotoxin polypeptide comprises an amino acid sequence of native chlorotoxin (SEQ ID NO: 1) in which:

(a) lysine residue K15, lysine residue K23, or a combination thereof are independently substituted with a basic or acidic amino acid, a non-polar or polar amino acid, a non-natural amino acid, an amino acid analog, or an amino acid mimetic thereof; or

(b) lysine residue K15, lysine residue K23, or a combination thereof are independently substituted with alanine or arginine.

3. The method of claim 1 , wherein the modified chlorotoxin polypeptide comprises a single lysine.

4. The method of claim 1 , wherein the modified chlorotoxin polypeptide is further conjugated to a therapeutic agent, a diagnostic agent, an imaging agent, a targeting agent, a moiety that increases circulatory half-life of the modified chlorotoxin polypeptide, or any combination thereof.

5. The method of claim 4 , wherein the therapeutic agent is a chemotherapeutic agent or a biological therapeutic agent.

6. The method of claim 4 , wherein the therapeutic agent is a cytotoxic agent.

7. The method of claim 4 , wherein the therapeutic agent is methotrexate, docetaxel, cisplatin, etoposide, cDNA, siRNA, shRNA, or RNAi.

8. The method of claim 4 , wherein the diagnostic or imaging agent is a fluorescent label, a radiolabel, or a magnetic resonance imaging label.

9. The method of claim 5 , wherein the biological therapeutic agent is a nucleic acid molecule, a transcription or translocation inhibitor, or a signal transduction modulator.

10. The method of claim 1 , wherein the chlorotoxin conjugate is further covalently conjugated to a therapeutic agent, a chemotherapeutic agent, a biological therapeutic agent, a cytotoxic agent, a moiety that increases the circulatory half-life of the modified chlorotoxin polypeptide, or any combination thereof.

11. The method of claim 1 , wherein the treating further comprises detecting the cancer cells.

12. The method of claim 11 , wherein the detecting comprises imaging the cancer cells.

13. The method of claim 11 , wherein the detecting further comprises measuring a level of binding of the chlorotoxin conjugate to the cancer cells as compared to normal tissue, wherein an elevated level of binding relative to normal tissue indicates the cells are cancerous.

14. The method of claim 11 , wherein the detecting further comprises differentiating cancer cells from normal tissue or determining location of cancer cells.

15. The method of claim 1 , wherein the treating further comprises removing or inhibiting the cancer cells detected by the chlorotoxin conjugate.

16. The method of claim 15 , wherein the removing comprises surgically removing the cancer cells.

17. The method of claim 15 , wherein the chlorotoxin conjugate is further covalently conjugated to a therapeutic agent, a chemotherapeutic agent, a biological therapeutic agent, a cytotoxic agent, a moiety that increases the circulatory half-life of the modified chlorotoxin polypeptide, or any combination thereof.

Assignments (3)
MERGER AND CHANGE OF NAME Recorded May 10, 2023
From: FRED HUTCHINSON CANCER RESEARCH CENTER; SEATTLE CANCER CARE ALLIANCE
To: FRED HUTCHINSON CANCER CENTER
Reel/Frame 063592/0512 →
MERGER AND CHANGE OF NAME Recorded Oct 6, 2022
From: FRED HUTCHINSON CANCER RESEARCH CENTER; FRED HUTCHINSON CANCER CENTER
To: FRED HUTCHINSON CANCER CENTER
Reel/Frame 061621/0059 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 9, 2022
From: OLSON, JAMES M.
To: FRED HUTCHINSON CANCER CENTER
Reel/Frame 061042/0413 →
Continuity (4)
Division 13673779 · Nov 9, 2012
Continuation PCTUS2011023797 · Feb 4, 2011
Provisional Application 61333556 · May 11, 2010
Related Publication 20180194818A1 · Jul 12, 2018