Method of treating a proliferative disease

US11007194B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11007194-B2
Application numberUS-201214355903-A
CountryUS
Kind codeB2
Filing dateNov 9, 2012
Priority dateNov 11, 2011
Publication dateMay 18, 2021
Grant dateMay 18, 2021

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention relates to a method of treating a patient with a serine/threonine kinase inhibitor wherein resistance to the treatment with a serine/threonine kinase inhibitor is suppressed by administering the serine/threonine kinase inhibitor on an intermittent dosing schedule.

First claim

Opening claim text (preview).

We claim: 1. A method of treating a proliferative disease in a subject in need thereof, wherein the proliferative disease is melanoma or colorectal cancer, and wherein the proliferative disease is characterized by a mutation in BRAF kinase, wherein the method comprises suppressing resistance to treatment with a BRAF inhibitor of the Formula II by administering the BRAF inhibitor of Formula II to the subject on an intermittent dosing schedule, wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 1, 2, 3, 4, 5, or 6 weeks followed by a period of 1, 2, 3, 4, 5, or 6 weeks without treatment. 2. A method of claim 1 wherein the BRAF mutation is a V600 mutation. 3. A method of claim 1 wherein the proliferative disease is melanoma which is characterized by a V600 mutation or colorectal cancer characterized by a V600 mutation. 4. A method of claim 1 wherein the proliferative disease is melanoma which is characterized by BRAFV600E or colorectal cancer characterized by BRAFV600E. 5. A method of claim 1 wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 4 weeks followed by a period of two weeks without treatment and repeating the cycle while the patient is treated with the BRAF inhibitor or until resistance emerges. 6. A method of claim 1 wherein the intermittent dosing schedule improves a therapeutic effect in tumor cells already resistant to treatment with the BRAF kinase inhibitor of Formula II. 7. The method of claim 1 , wherein the proliferative disease is a tumor. 8. The method of claim 7 , wherein said tumor is melanoma which is characterized by a V600 mutation. 9. The method of claim 8 , wherein said tumor is melanoma which is characterized by a V600E mutation. 10. The method of claim 8 , wherein the BRAF inhibitor of Fomula II is administered once daily during the period of administration of the BRAF inhibitor of Formula II. 11. The method of claim 9 , wherein the BRAF inhibitor of Formula II is administered once daily during the period of administration of the BRAF inhibitor of Formula II. 12. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor of Formula II for a period of 4 weeks followed by a period of 2 weeks wherein treatment with the BRAF inhibitor of Formula II is withheld, and repeating the cycle while the patient is treated with the BRAF inhibitor of Formula II. 13. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 1 week followed by a period of 1 week wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 14. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 2 weeks followed by a period of 1 week wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 15. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 2 weeks followed by a period of 2 weeks wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 16. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 3 weeks followed by a period of 1 week wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 17. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 3 weeks followed by a period of 2 weeks wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 18. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 3 weeks followed by a period of 3 weeks wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 19. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 4 weeks followed by a period of 1 week wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 20. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 4 weeks followed by a period of 3 weeks wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 21. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 4 weeks followed by a period of 4 weeks wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 22. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 5 weeks followed by a period of 1 week wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 23. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 5 weeks followed by a period of 2 weeks wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 24. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 5 weeks followed by a period of 3 weeks wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 25. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 5 weeks followed by a period of 4 weeks wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 26. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 5 weeks followed by a period of 5 weeks wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 27. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a period of 6 weeks followed by a period of 1 week wherein treatment with the BRAF inhibitor of Formula II is withheld and repeating the cycle while the patient is treated with the BRAF inhibitor. 28. The method of claim 11 , wherein the intermittent dosing schedule comprises administering the BRAF inhibitor for a

Assignees

Inventors

Classifications

  • Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

  • A61K31/506Primary

    not condensed and containing further heterocyclic rings · CPC title

  • Antineoplastic agents · CPC title

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Frequently asked questions

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What does patent US11007194B2 cover?
The present invention relates to a method of treating a patient with a serine/threonine kinase inhibitor wherein resistance to the treatment with a serine/threonine kinase inhibitor is suppressed by administering the serine/threonine kinase inhibitor on an intermittent dosing schedule.
Who is the assignee on this patent?
Array Biopharma Inc
What technology area does this patent fall under?
Primary CPC classification A61K31/506. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue May 18 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).