IP Library › Granted Patent US 10,994,033
Granted Patent B2
US 10,994,033 · App. 16/305,286 · Granted May 4, 2021

Imaging methods using 18F-radiolabeled biologics

Inventors: David Donnelly (Doylestown, PA); David K. Leung (West Windsor, NJ)
Assignee: BRISTOL-MYERS SQUIBB COMPANY
A61K51/088A61K49/0004C07K16/2818
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,994,033
App. No.
16/305,286
Granted
May 4, 2021
Kind
B2
Abstract

The invention relates to water soluble 18 F-prosthetic groups and the synthesis and use 18 F-labeled biological molecules containing the 18 F-prosthetic groups for imaging various processes within the body, for detecting the location of molecules associated with disease pathology, and for monitoring disease progression are disclosed.

Claims (35)

1. A method of visualizing a target molecule in a subject, comprising

a. administering to the subject an imaging agent that binds specifically to the target molecule at a dose of about 3-10 mCi (100-333 MBq); and

b. conducting a PET scan of the subject about 30-120 minutes after step (a), wherein the imaging agent comprises

(i) an 18 F-radiolabeled prosthetic group comprising the structure

or a pharmaceutically acceptable salt thereof, wherein x is an integer from 1 to 8 the 18 F-radiolabel is attached ortho to the N atom of the pyridine; and

(ii) a protein linked to the 18 F-radiolabeled prosthetic group by a bifunctional conjugating (BFC) moiety, wherein the protein is an antibody, an antigen binding fragment of an antibody, or a fibronectin type III (Fn3) domain.

2. The method of claim 1 , wherein the subject has at least one tumor.

3. The method of claim 2 , comprising determining the level of the target molecule in the at least one tumor of the subject.

4. The method of claim 3 , wherein the level of target molecule in the at least one tumor is indicative of whether a subject is likely to respond to a treatment with an immuno-oncology agent.

5. The method of claim 4 , wherein the target molecule is human PD-L1, and the immune-oncology agent is a PD-1 or PD-L1 antagonist.

6. The method of claim 5 , wherein the PD-1 antagonist is an anti-PD-1 antibody.

7. The method of claim 1 , wherein the 18 F-radiolabeled prosthetic group comprises the structure

or a pharmaceutically acceptable salt thereof.

8. The method of claim 1 , wherein the 18 F-radiolabeled prosthetic group comprises the structure

or a pharmaceutically acceptable salt thereof.

9. The method of claim 1 , wherein the 18 F-radiolabeled prosthetic group comprises the structure

or a pharmaceutically acceptable salt thereof.

10. The method of claim 1 , wherein the 18 F-radiolabeled prosthetic group is linked to a fibronectin type III (Fn3) domain.

11. The method of claim 10 , wherein 18 F-radiolabeled prosthetic group comprises the following structure,

12. The method of claim 10 , wherein 18 F-radiolabeled prosthetic group comprises the following structure,

13. The method of claim 10 , wherein the 18 F-radiolabeled prosthetic group has the structure

14. The method of claim 10 , wherein the imaging agent has the following structure,

wherein the maleimide group of the BFC is covalently linked to the thiol group on a cysteine residue of the protein.

15. The method of claim 14 , wherein the cysteine residue is at the C-terminus of the protein.

16. The method of claim 1 , wherein the target molecule is associated with a disease.

17. The method of claim 1 , wherein the Fn3 domain is a human 10 Fn3 domain.

18. The method of claim 1 , wherein the BFC comprises a cyclooctyne selected from the group consisting of a dibenzocyclooctyne, a biarylazacyclooctynone and a dimethoxyazacyclooctyne.

19. The method of claim 18 , wherein the BFC is DBCO-PEG4-NHS-Ester, DBCO-Sulfo-NHS-Ester, DBCO-PEG4-Acid, DBCO-PEG4-Amine or DBCO-PEG4-Maleimide.

20. A method of visualizing a target molecule in a subject, comprising

a. administering to the subject an imaging agent that binds specifically to the target molecule at a dose of about 3-10 mCi (100-333 MBq); and

b. conducting a PET scan of the subject about 30-120 minutes after step (a), wherein the imaging agent comprises

(i) an 18 F-radiolabeled prosthetic group having the structure

wherein “OPEG” is [O(CH 2 ) 2 ] x , and x is an integer from 1 to 8, or a pharmaceutically acceptable salt thereof, and

(ii) a protein linked to the 18 F-radiolabeled prosthetic group by a bifunctional conjugating (BFC) moiety, wherein the protein is an antibody, an antigen binding fragment of an antibody, or a fibronectin type III (Fn3) domain.

21. The method of claim 20 , wherein the 18 F-radiolabeled prosthetic group is linked to a fibronectin type III (Fn3).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 28, 2020
From: DONNELLY, DAVID; LEUNG, DAVID K.
To: BRISTOL-MYERS SQUIBB COMPANY
Reel/Frame 052775/0060 →
Continuity (2)
Provisional Application 62344289 · Jun 1, 2016
Related Publication 20190184043A1 · Jun 20, 2019
Cited By (2)
US 12,194,110 US 12,529,165