You’re using a public version of DrugPatentWatch with 5 free searches available | Register to unlock more free searches. CREATE FREE ACCOUNT

Last Updated: April 25, 2024

Claims for Patent: 9,415,103


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 9,415,103
Title:Combination therapy to prevent DCIS formation and progression to breast cancer
Abstract: A method of treating a ductal carcinoma in situ (DCIS) lesion in a subject in need thereof is disclosed. The method comprises administering to the subject a therapeutically effective amount of a first agent capable of down-regulating activity and/or expression of at least one component participating in a NOTCH pathway, and a second agent capable of down-regulating an activity and/or expression of HER2, thereby treating the DCIS lesion.
Inventor(s): Yarden; Yosef (Rehovot, IL), Chaluvally-Raghavan; Pradeep (Rehovot, IL)
Assignee: Yeda Research and Development Co. Ltd. (Rehovot, IL)
Application Number:14/125,588
Patent Claims:1. A method of treating a ductal carcinoma in situ (DCIS) lesion in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of a first agent capable of down-regulating activity and/or expression of at least one component participating in a NOTCH pathway, and a second agent capable of down-regulating an activity and/or expression of HER2, wherein said second agent is an antibody, thereby treating the DCIS lesion.

2. The method of claim 1, further comprising analyzing in a breast sample of said subject an expression of said at least one component participating in a NOTCH pathway, prior to said treating.

3. The method of claim 2, further comprising analyzing in a breast sample of said subject an expression of HER2 prior to said treating.

4. The method of claim 1, further comprising analyzing in a breast sample of said subject an expression of HER2 prior to said treating.

5. The method of claim 1, wherein said antibody comprises Trastuzumab.

6. The method of claim 1, wherein said at least one component is selected from the group consisting of Hairy and Enhancer of Split 1(HES1), NOTCH 2, NOTCH 3, ADAM17 and Presenilin1.

7. The method of claim 1, wherein said at least one component is NOTCH3.

8. The method of claim 1, wherein said first agent is an siRNA molecule.

9. The method of claim 1, wherein said first agent is a gamma secretase inhibitor, a mitogen-activated protein kinase (MEK) specific inhibitor or a PI3K-AKT inhibitor.

10. The method of claim 9, wherein said first agent is a gamma secretase inhibitor.

11. A method of treating a ductal carcinoma in situ (DCIS) lesion in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of a first agent selected from the group consisting of an antibody, an RNA silencing agent and an antagonist molecule capable of down-regulating activity and/or expression of at least one component participating in a NOTCH pathway selected from the group consisting of a NOTCH receptor, NOTCH ligand, NOTCH receptor intracellular domain (NICD), ADM17, presenilinl, HES, HERP, HEY, RBPSUH, Su(H), Lag-1, c-Myc and Cyclin D1, gamma-secretase, mitogen-activated protein kinase (MEK) and PI3K-AKT, and a second agent selected from the group consisting of an antibody, an RNA silencing agent and a kinase inhibitor molecule capable of down-regulating an activity and/or expression of HER2, thereby treating the DCIS lesion.

12. The method of claim 11, further comprising analyzing in a breast sample of said subject an expression of said at least one component participating in a NOTCH pathway, prior to said treating.

13. The method of claim 12, further comprising analyzing in a breast sample of said subject an expression of HER2 prior to said treating.

14. The method of claim 11, further comprising analyzing in a breast sample of said subject an expression of HER2 prior to said treating.

15. The method of claim 11, wherein said second agent is an antibody.

16. The method of claim 15, wherein said antibody comprises Trastuzumab.

17. The method of claim 11, wherein said second agent is a kinase inhibitor.

18. The method of claim 17, wherein said kinase inhibitor is lapatinib.

19. The method of claim 11, wherein said at least one component is selected from the group consisting of Hairy and Enhancer of Split 1 (HES1), NOTCH 2, NOTCH 3, ADAM17 and Presenilin1.

20. The method of claim 11, wherein said at least one component is NOTCH3.

21. The method of claim 11, wherein said first agent is an siRNA molecule.

22. The method of claim 11, wherein said first agent is a gamma secretase inhibitor, a mitogen-activated protein kinase (MEK) specific inhibitor or a PI3K-AKT inhibitor.

23. The method of claim 11, wherein said first agent is a gamma secretase inhibitor.

Details for Patent 9,415,103

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Genentech, Inc. HERCEPTIN trastuzumab For Injection 103792 09/25/1998 ⤷  Try a Trial 2031-06-14
Genentech, Inc. HERCEPTIN trastuzumab For Injection 103792 02/10/2017 ⤷  Try a Trial 2031-06-14
Genentech, Inc. HERCEPTIN HYLECTA trastuzumab and hyaluronidase-oysk Injection 761106 02/28/2019 ⤷  Try a Trial 2031-06-14
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.