IP Library Patent Application 18876651
Patent Application
App. No. 18/876,651

METHODS OF TREATING GLIOBLASTOMA WITH PRODRUGS OF RILUZOLE

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Patent No.
US None
App. No.
18/876,651
Abstract

Provided is a method of treating glioblastoma in a patient in need of such treatment, comprising administering to the patient a first dosage form comprising a therapeutically active amount of troriluzole or a pharmaceutically acceptable salt thereof.

Claims (34)

1 . A method of treating glioblastoma in a patient in need of such treatment, comprising administering to the patient a first dosage form comprising a therapeutically active amount of troriluzole or a pharmaceutically acceptable salt thereof.

2 . The method according to claim 1 , wherein the first dosage form comprises 100 mg of troriluzole or an equivalent amount of a pharmaceutically acceptable salt thereof.

3 . The method according to claim 1 or 2 , wherein the first dosage form comprises 200 mg of troriluzole or an equivalent amount of a pharmaceutically acceptable salt thereof.

4 . The method according to any one of claims 1 to 3 , wherein the first dosage form is administered once a day.

5 . The method according to any one of claims 1 to 4 , wherein the first dosage form is administered twice a day.

6 . The method according to any one of claims 1 to 5 , wherein the duration of treatment is four weeks, and wherein troriluzole or a pharmaceutically acceptable salt thereof is administered in an amount of 100 mg twice a day for the first two weeks and in amount of 200 mg twice a day for the other two weeks.

7 . The method according to any one of claims 1 to 6 , wherein the total amount of troriluzole or a pharmaceutically acceptable salt thereof administered to the patient during the day is 200 mg.

8 . The method according to any one of claims 1 to 7 , wherein the total amount of troriluzole or a pharmaceutically acceptable salt thereof administered to the patient during the day is 300 mg.

9 . The method according to any one of claims 1 to 8 , wherein the total amount of troriluzole or a pharmaceutically acceptable salt thereof administered to the patient during the day is 400 mg.

10 . The method according to any one of claims 1 to 9 , further comprising administering to the patient a second dosage form comprising a therapeutically active amount of temozolomide or a pharmaceutically acceptable salt thereof.

11 . The method according to claim 10 , wherein the second dosage form comprises 75 mg of temozolomide or an equivalent amount of a pharmaceutically acceptable salt thereof.

12 . The method according to claim 10 or 11 , wherein the second dosage form comprises 150 mg of temozolomide or an equivalent amount of a pharmaceutically acceptable salt thereof.

13 . The method according to any one of claims 10 to 12 , wherein the second dosage form is administered once a day.

14 . The method according to any one of claims 10 to 13 , wherein the second dosage form is administered twice a day.

15 . The method according to any one of claims 10 to 14 , wherein the total amount of temozolomide or a pharmaceutically acceptable salt thereof administered to the patient during the day is 75 mg.

16 . The method according to any one of claims 10 to 15 , wherein the total amount of temozolomide or a pharmaceutically acceptable salt thereof administered to the patient during the day is 150 mg.

17 . The method according to any one of claims 1 to 16 , wherein the glioblastoma is newly diagnosed O 6 -methylguanine-DNA-methyltransferase (MGMT) methylated glioblastoma.

18 . The method according to any one of claims 1 to 16 , wherein the glioblastoma is newly diagnosed O 6 -methylguanine-DNA-methyltransferase (MGMT) unmethylated glioblastoma.

19 . The method according to claim 1 , further comprising administering to the patient a third dosage form comprising a therapeutically active amount of lomustine or an equivalent amount of a pharmaceutically acceptable salt thereof.

20 . The method according to claim 19 , wherein the third dosage form comprises 50 mg of lomustine or an equivalent amount of a pharmaceutically acceptable salt thereof.

21 . The method according to claim 19 or 20 , wherein the third dosage form comprises 100 mg of lomustine or an equivalent amount of a pharmaceutically acceptable salt thereof.

22 . The method according to any one of claims 19 to 21 , wherein the third dosage form is administered once a day.

23 . The method according to any one of claims 19 to 22 , wherein the third dosage form is administered twice a day.

24 . The method according to any one of claims 19 to 23 , wherein the total amount of lomustine or a pharmaceutically acceptable salt thereof administered to the patient during the day is 100 mg.

25 . The method according to any one of claims 19 to 24 , wherein the glioblastoma is recurring glioblastoma.

26 . The method according to any one of claims 1 to 25 , further comprising irradiating glioblastoma cells with a therapeutically effective dose of ionizing radiation.

27 . A kit for use in a method of treating a patient afflicted with glioblastoma, the kit comprising:

(a) troriluzole or a pharmaceutically acceptable salt thereof;

(b) temozolomide or a pharmaceutically acceptable salt thereof; and

(b) instructions for administering troriluzole and temozolomide according to the method of any of claims 1 - 26 .

27 . A kit for use in a method of treating a patient afflicted with glioblastoma, the kit comprising:

(a) troriluzole or a pharmaceutically acceptable salt thereof;

(b) lomustine or a pharmaceutically acceptable salt thereof; and

(b) instructions for administering troriluzole and temozolomide according to the method of any of claims 1 - 26 .

Assignments (1)
SECURITY INTEREST Recorded May 1, 2025
From: BIOHAVEN THERAPEUTICS LTD
To: BEETLEJUICE SA LLC, AS PURCHASER AGENT
Reel/Frame 071147/0260 →