Cytotoxic and anti-mitotic compounds, and methods of using the same
Compounds having cytotoxic and/or anti-mitotic activity are disclosed. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed. Also disclosed are compositions having the structure: (T)-(L)-(D), wherein (T) is a targeting moiety, (L) is an optional linker, and (D) is a compound having cytotoxic and/or anti-mitotic activity.
1. A conjugate of Formula II:
(T)-(L)-(D) II
wherein:
(T) is an antibody that specifically binds HER2, and
(L)-(D) has the structure:
wherein n is 1, 2, 3 or 4.
2. A pharmaceutical composition comprising the conjugate of claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, diluent or excipient.
3. A method of inhibiting tumor growth in a human subject comprising administering to a human subject in need thereof an effective amount of a conjugate of claim 1 .
4. The conjugate of claim 1 , wherein (T) is a bispecific antibody.
5. A pharmaceutical composition comprising the conjugate of claim 4 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, diluent or excipient.
6. A method of inhibiting tumor growth in a human subject comprising administering to a human subject in need thereof an effective amount of a conjugate of claim 4 .
7. A method of increasing survival of a human subject having cancer comprising administering to the human subject an effective amount of a conjugate of claim 1 .
8. A method of increasing survival of a human subject having cancer comprising administering to the human subject an effective amount of a conjugate of claim 4 .
9. The pharmaceutical composition according to claim 2 , formulated for parenteral administration.
10. The pharmaceutical composition according to claim 5 , formulated for parenteral administration.
11. The method according to claim 3 , wherein the conjugate is administered to the human subject parenterally.
12. The method according to claim 6 , wherein the conjugate is administered to the human subject parenterally.
13. The method according to claim 7 , wherein the conjugate is administered to the human subject parenterally.
14. The method according to claim 8 , wherein the conjugate is administered to the human subject parenterally.
15. The method according to claim 3 , wherein the tumor is a solid tumor or a lymphoma.
16. The method according to claim 6 , wherein the tumor is a solid tumor or a lymphoma.
17. The method according to claim 7 , wherein the cancer is a solid tumor or a lymphoma.
18. The method according to claim 8 , wherein the cancer is a solid tumor or a lymphoma.