IP Library Granted Patent US 11,951,080
Granted Patent B2
US 11,951,080 · App. 18/066,694 · Granted Apr 9, 2024

Method of treating cancer using selective estrogen receptor modulators

Inventors: Suzanne E. Wardell (Durham, NC); Erik R. Nelson (Champaign, IL); Donald P. McDonnell (Chapel Hill, NC)
Assignee: Duke University
A61K31/137A61K9/0019A61K31/136A61K31/138A61K31/40A61K31/4196A61K31/4535A61K31/565A61K31/5685A61K45/06C07C217/78C07C217/84A61K2121/00A61P35/00
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Quick Facts
Patent No.
US 11,951,080
App. No.
18/066,694
Granted
Apr 9, 2024
Kind
B2
Abstract

Disclosed herein are methods of treating subjects suffering from estrogen receptor positive cancer of the brain by administering a selective estrogen receptor degrader (SERM). Also disclosed are methods of treating a cancer that is resistant to an estrogen receptor modulator by administering a SERM.

Claims (11)

1. A method of treating ovarian cancer in a subject, the method comprising administering a compound of (R)-6-{2-{ethyl[4-(2-ethylaminoethyl)benzyl]amino}-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-ol, wherein the ovarian cancer is estrogen receptor positive, and is resistant to an estrogen receptor modulator.

2. The method of claim 1 , wherein an effective amount of the compound is administered.

3. The method of claim 2 , wherein the effective amount comprises a high dosage.

4. The method of claim 3 , wherein the high dosage is more than about 20 mg/kg.

5. The method of claim 3 , wherein the high dosage is about 20 mg/kg to about 100 mg/kg.

6. The method of claim 1 , wherein the compound is administered by oral administration, intravenous administration, intradermal injection, intramuscular injection, or subcutaneous injection.

7. The method of claim 1 , further comprising administering an effective amount of at least one compound selected from the group consisting of a cyclin-dependent kinase 4 and 6 inhibitor (CDK4/6 inhibitor), an antiestrogen, a ligand of retinoic acid or retinoxic X receptor, an antiprogestin, an antiandrogen, vitamin D or metabolite thereof, a farnesyl transferase inhibitor, a PPARa or gamma agonist and a MAP kinase inhibitor.

8. The method of claim 1 , wherein the ovarian cancer is de novo resistant to the estrogen receptor modulator.

9. The method of claim 1 , wherein the resistance to the estrogen receptor modulator is acquired.

10. The method of claim 1 , wherein the estrogen receptor modulator is a selective estrogen receptor modulator (SERM).

11. The method of claim 10 , wherein the SERM is tamoxifen, idoxifene, raloxifene, or ICI 182,780.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 16, 2022
From: WARDELL, SUZANNE E.; NELSON, ERIK R.; MCDONNELL, DONALD P.
To: DUKE UNIVERSITY
Reel/Frame 062120/0247 →