IP Library Granted Patent US 9,675,600
Granted Patent B2
US 9,675,600 · App. 14/839,038 · Granted Jun 13, 2017

Medical treatments based on anamorelin

Inventors: William Mann (Hoboken, NJ); John Friend (Colts Neck, NJ); William Polvino (Tinton Falls, NJ); Suzan Allen (Georgetown, TX); Ming Lu (Plainsboro, NJ); Elizabeth Duus (Hatboro, PA); Ruben Giorgino (Allschwil, CH); Enrico Baroni (Cernobbio, IT)
Assignee: HELSINN HEALTHCARE SA
A61K31/454A61K31/00
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Quick Facts
Patent No.
US 9,675,600
App. No.
14/839,038
Granted
Jun 13, 2017
Kind
B2
Abstract

Methods of treating cancer related conditions using anamorelin are described.

Claims (25)

1. A method of treating weight loss in a human cancer patient, wherein said patient has a body mass index less than 20 kg/m 2 and a weight loss greater than 2% in the previous 6 months, comprising administering to said patient 100 mg of anamorelin or a pharmaceutically acceptable salt thereof once daily for a therapeutically effective period of time.

2. A method of treating early satiety in a human cancer patient, wherein said patient has a body mass index less than 20 kg/m 2 and a weight loss greater than 2% in the previous 6 months, comprising administering to said patient 100 mg of anamorelin or a pharmaceutically acceptable salt thereof once daily for a therapeutically effective period of time.

3. A method of treating fatigue in a human cancer patient, wherein said patient has a body mass index less than 20 kg/m 2 and a weight loss greater than 2% in the previous 6 months, comprising administering to said patient 100 mg of anamorelin or a pharmaceutically acceptable salt thereof once daily for a therapeutically effective period of time.

4. A method of improving quality of life as measured by FAACT in the anorexia/cachexia domain in a human cancer patient, wherein said patient has a body mass index less than 20 kg/m 2 and a weight loss greater than 2% in the previous 6 months, comprising administering to said patient 100 mg of anamorelin or a pharmaceutically acceptable salt thereof once daily for a therapeutically effective period of time.

5. The method of claim 3 wherein said fatigue is caused by depression, anemia, sarcopenia, anorexia, vomiting-related malnutrition, chemo-toxicity, opioid use, and/or sleep disturbances.

6. The method of claim 1 wherein said human cancer patient is suffering from unresectable Stage III or IV non-small cell lung cancer.

7. The method of claim 1 wherein said therapeutically effective amount of anamorelin comprises 100 mg of anamorelin HCl based on the weight of the salt.

8. The method of claim 1 wherein said therapeutically effective amount of anamorelin comprises 100 mg of anamorelin HCl based on the weight of the salt administered orally once daily at least one hour before the first meal.

9. The method of claim 1 wherein said therapeutically effective amount of anamorelin is effective to increase lean body mass of said patient.

10. The method of claim 1 wherein said therapeutically effective amount of anamorelin is effective to increase total body mass and lean body mass in said patient.

11. The method of claim 1 wherein said therapeutically effective amount of anamorelin is effective to increase total body mass, lean body mass and fat mass of said patient.

12. The method of claim 1 wherein said therapeutically effective period of time is from 13 to 24 weeks.

13. The method of claim 1 wherein said patient has a performance status on the ECOG scale of 2 or higher.

14. The method of claim 1 wherein said patient has a squamous tumor histology.

15. The method of claim 1 wherein said cancer has metasticized.

16. The method of claim 1 wherein said patient is not receiving chemotherapy or radiotherapy.

17. The method of claim 1 wherein said patient is receiving chemotherapy or radiotherapy.

18. The method of claim 1 wherein said patient is receiving opioids and/or antiemetics.

19. The method of claim 2 wherein said human cancer patient is suffering from unresectable Stage III or IV non-small cell lung cancer.

20. The method of claim 3 wherein said human cancer patient is suffering from unresectable Stage III or IV non-small cell lung cancer.

21. The method of claim 4 wherein said human cancer patient is suffering from unresectable Stage III or IV non-small cell lung cancer.

22. The method of claim 1 , wherein said treatment is effective for 9 consecutive weeks.

23. The method of claim 2 , wherein said treatment is effective for 9 consecutive weeks.

24. The method of claim 3 , wherein said treatment is effective for 9 consecutive weeks.

25. The method of claim 4 , wherein said treatment is effective for 9 consecutive weeks.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Sep 20, 2023
From: HAMILTON SA LLC
To: HELSINN HEALTHCARE SA; HELSINN THERAPEUTICS (U.S.), INC.; HELSINN BIREX PHARMACEUTICALS LIMITED
Reel/Frame 064961/0567 →
SECURITY INTEREST Recorded Dec 30, 2022
From: HELSINN HEALTHCARE SA; HELSINN THERAPEUTICS (U.S.), INC.; HELSINN BIREX PHARMACEUTICALS LIMITED
To: HAMILTON SA LLC
Reel/Frame 062254/0888 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 7, 2017
From: GIORGINO, RUBEN; BARONI, ENRICO
To: HELSINN HEALTHCARE SA
Reel/Frame 041487/0164 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 11, 2016
From: MANN, WILLIAM; FRIEND, JOHN; LU, MING; DUUS, ELIZABETH; POLVINO, WILLIAM; ALLEN, SUZAN
To: HELSINN HEALTHCARE SA
Reel/Frame 038545/0293 →
Continuity (2)
Provisional Application 62045976 · Sep 4, 2014
Related Publication 20160067236A1 · Mar 10, 2016