Labeled inhibitors of prostate specific membrane antigen (PSMA) as agents for the treatment of prostate cancer
The present invention generally relates to the field of radiopharmaceuticals and their use in nuclear medicine as tracers, imaging agents and for the treatment of various disease states of prostate cancer. Thus, the present invention concerns compounds that are represented by the general Formulae (Ia) or (Ib).
1. A compound of the formula:
or a salt thereof,
wherein R′ is a chelator of the formula:
and
wherein 90 Y is complexed to the chelator.
2. A composition comprising:
(1) the compound and/or a salt thereof according to claim 1 ; and
(2) optionally a pharmaceutically acceptable carrier.
3. The composition of claim 2 , wherein the composition further comprises an excipient, and wherein the excipient is different from said pharmaceutically acceptable carrier.
4. The composition of claim 2 , wherein the composition is a buffered solution.
5. The composition of claim 2 , wherein the pharmaceutically acceptable carrier is selected from mannitol, lactose, glucose, albumin, or a combination thereof.
6. A compound of the formula:
or a salt thereof,
wherein R′ is a chelator of the formula:
and
wherein 90 Y is complexed to the chelator.
7. A composition comprising:
(1) the compound and/or a salt thereof according to claim 6 ; and
(2) optionally a pharmaceutically acceptable carrier.
8. The composition of claim 7 , wherein the composition further comprises an excipient, and wherein the excipient is different from said pharmaceutically acceptable carrier.
9. The composition of claim 7 , wherein the composition is a buffered solution.
10. The composition of claim 7 , wherein the pharmaceutically acceptable carrier is selected from mannitol, lactose, glucose, and albumin.
11. A compound of the formula:
or a salt thereof,
wherein R′ is a chelator of the formula:
and
wherein 90 Y is complexed to the chelator.
12. A composition comprising:
(1) the compound and/or a salt thereof according to claim 11 ; and
(2) optionally a pharmaceutically acceptable carrier.
13. The composition of claim 12 , wherein the composition further comprises an excipient, and wherein the excipient is different from said pharmaceutically acceptable carrier.
14. The composition of claim 12 , wherein the composition is a buffered solution.
15. The composition of claim 12 , wherein the pharmaceutically acceptable carrier is selected from mannitol, lactose, glucose, albumin, or a combination thereof.