US2023025971A1PendingUtilityA1
Methods for treating cancer
Est. expiryMay 10, 2039(~12.8 yrs left)· nominal 20-yr term from priority
A61K 9/0019A61K 47/26A61K 38/12A61K 47/183A61P 35/00C07K 16/2818A61K 2039/505A61K 39/3955A61K 31/337A61K 38/10A61K 38/08A61K 39/39541A61K 2300/00A61K 45/06
69
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Claims
Abstract
The present invention relates to a method of treating a cancer in a patient.
Claims
exact text as granted — not AI-modified1 . A method of treating a cancer in a patient, comprising administering to said patient a therapeutically effective amount of BT1718, or a pharmaceutically acceptable salt thereof, and a checkpoint inhibitor, wherein the cancer is a colon cancer, and wherein the checkpoint inhibitor is a CTLA-4 antagonist.
2 - 14 . (canceled)
15 . The method of claim 1 , wherein the method comprises administering BT1718, or a pharmaceutically acceptable salt thereof, at a dose of about 19.2 mg/m 2 .
16 . The method of claim 1 , wherein the method comprises administering BT1718, or a pharmaceutically acceptable salt thereof, at a frequency of once a week.
17 . The method of claim 1 , wherein the CTLA-4 antagonist is an anti-CTLA4 antibody.
18 . The method of claim 1 , wherein BT1718, or a pharmaceutically acceptable salt thereof, is administered by an intravenous infusion.
19 - 22 . (canceled)
23 . The method of claim 1 , wherein the method comprises administering BT1718, or a pharmaceutically acceptable salt thereof, at a dose of about 14.4 mg/m 2 .
24 . The method of claim 1 , wherein the method comprises administering BT1718, or a pharmaceutically acceptable salt thereof, at a dose of about 18.6 mg/m 2 .
25 . The method of claim 1 , wherein the method comprises administering BT1718, or a pharmaceutically acceptable salt thereof, at a dose of about 14-24 mg/m 2 .
26 . The method of claim 1 , wherein the method comprises administering BT1718, or a pharmaceutically acceptable salt thereof, at a dose of about 9-18 mg/m 2 .
27 . The method of claim 1 , wherein the method comprises administering BT1718, or a pharmaceutically acceptable salt thereof, at a frequency of once every 1.5 weeks.
28 . The method of claim 1 , wherein the method comprises administering BT1718, or a pharmaceutically acceptable salt thereof, at a frequency of once every 2 weeks.
29 . The method of claim 1 , wherein the method comprises administering BT1718, or a pharmaceutically acceptable salt thereof, at a frequency of once every 2.5 weeks.
30 . The method of claim 1 , wherein the method comprises administering BT1718, or a pharmaceutically acceptable salt thereof, at a frequency of once every 3 weeks.
31 . The method of claim 1 , wherein the method comprises administering BT1718, or a pharmaceutically acceptable salt thereof, at a frequency of once every 4 weeks.
32 . The method of claim 17 , wherein the anti-CTLA4 antibody is ipilimumab.
33 . The method of claim 17 , wherein the anti-CTLA4 antibody is tremelimumab.
34 . The method of claim 1 , wherein BT1718, or a pharmaceutically acceptable salt thereof, is administered with histidine.
35 . The method of claim 1 , wherein BT1718, or a pharmaceutically acceptable salt thereof, is administered with sucrose.
36 . The method of claim 1 , wherein BT1718, or a pharmaceutically acceptable salt thereof, is administered by an about 1 hour intravenous infusion.
37 . The method of claim 1 , wherein BT1718, or a pharmaceutically acceptable salt thereof, is administered with the CTLA-4 antagonist simultaneously or sequentially in separate unit dosage forms.Cited by (0)
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