IP Library Granted Patent US 9,616,072
Granted Patent B2
US 9,616,072 · App. 14/853,130 · Granted Apr 11, 2017

Reduction of side effects from aromatase inhibitors used for treating breast cancer

Inventor: Stephen Nigel Birrell (Medindie, AU)
Assignee: CHAVAH PTY LTD.
A61K31/568A61K9/0019A61K9/0053A61K9/20A61K31/4196A61K45/06
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Quick Facts
Patent No.
US 9,616,072
App. No.
14/853,130
Granted
Apr 11, 2017
Kind
B2
Abstract

The present invention is directed generally to pharmaceutical compositions, methods, and kits for improving side effects associated with aromatase inhibitor treatment in a subject diagnosed with breast cancer. More specifically, the present invention provides compositions, methods, and kits comprising an aromatase inhibitor and an androgenic agent.

Claims (19)

1. A method of mitigating one or more side effects in a perimenopausal or a postmenopausal patient being treated for breast cancer, comprising administering to said patient:

a) an effective amount of an androgenic agent; and

b) an effective amount of an aromatase inhibitor;

wherein the mitigated one or more side effects comprises breast pain, arthritis or arthralgia.

2. The method of claim 1 , wherein the aromatase inhibitor is a nonsteroidal aromatase inhibitor.

3. The method of claim 2 , wherein the nonsteroidal aromatase inhibitor is selected from a group consisting of anastrozole, letrozole, vorozole or fadrozole.

4. The method of claim 3 , wherein the aromatase inhibitor is anastrozole that is administered subcutaneously.

5. The method of claim 3 , wherein the androgenic agent and the aromatase inhibitor are administered subcutaneously.

6. The method of claim 3 , wherein the androgenic agent and the aromatase inhibitor are administered orally in tablet form.

7. The method of claim 3 , wherein the androgenic agent increases androgenic activity or binds to the androgen receptor in said patient.

8. The method of claim 3 , wherein the androgenic agent is testosterone.

9. The method of claim 1 , wherein the aromatase inhibitor treatment is an adjuvant therapy treatment to said patient already having received chemotherapy.

10. The method of claim 1 , wherein the aromatase inhibitor blocks conversion of said testosterone to estrogen.

11. The method of claim 10 , wherein the conversion is blocked in small bowel lymphatics and liver.

12. The method of claim 1 , wherein either or both the androgenic agent and the aromatase inhibitor are administered orally, intraperitoneally, intradermally, transdermally, transmucosally, subcutaneously, sublingually, intravenously, intraarterially, intracavity, intracranially, intramuscularly, parenterally, or topically, or a combination thereof.

13. The method of claim 1 , wherein the one or more side effects further comprises: vasodilatation, osteoporosis, osteopenia, loss of libido, weight gain, vaginal dryness, sleeping difficulties, night sweats, asthenia, painful intercourse, pain, pharyngitis, depression, bloating, nausea, rash, mood swings, headache, hypertension, insomnia, lymphoedema, back pain, peripheral edema, cold sweats, abdominal pain, injury, constipation, coughing, diarrhea, fracture, hypercholesteremia, infection, arthrosis, dizziness, dyspnea, paresthesia, urinary tract infection, vulvovaginitis, anxiety, bone pain, chest pain, dyspepsia, flu syndrome, gastrointestinal disorder, sweating, or leukorrhea.

14. The method of claim 1 , wherein the androgenic agent is selected from the group consisting of: testosterone, methyltestosterone, androstenediol, androstenediol-3-acetate, androstenediol-17- acetate, androstenediol-3,17-diacetate, androstenediol-17-benzoate, androstenediol- 3-acetate-17-benzoate, androstenedione, adrenosterone, androsterone acetate, androsterone propionate, androsterone benzoate, dehydroepiandrosterone, sodium dehydroepiandrosterone sulfate, oxymetholone, fluoxymesterone, methandrostenolone, testolactone, pregnenolone, 17α-methylnortestosterone, norethandrolone, dihydrotestosterone, 5α-dihydrotestosterone, dromostanolone, dromostanolone propionate, nandrolone, nandrolone phenpropionate, nandrolone decanoate, nandrolone furylpropionate, nandrolone cyclohexanepropionate, nandrolone benzoate, nandrolone cyclohexanecarboxylate, danazol, oxymetholone, androsterone, stanozolol, ethylestrenol, oxandrolone, bolasterone, mesterolone, testosterone propionate, testosterone cypionate, testosterone phenylacetate, testosterone enanthate, testosterone acetate, testosterone buciclate, testosterone heptanoate, testosterone decanoate, testosterone undecanoate, testosterone caprate, testosterone isocaprate, and combinations thereof.

15. The method of claim 1 , wherein the androgenic agent is testosterone, testosterone undecanoate, methyltestosterone, or di-hydrotestosterone.

16. The method of claim 1 , wherein the androgenic agent and the aromatase inhibitor are administered orally in tablet form.

Assignments (2)
CHANGE OF NAME Recorded Sep 7, 2017
From: CHAVAH PTY LTD.
To: HAVAH THERAPEUTICS PTY LTD.
Reel/Frame 043525/0633 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2015
From: BIRRELL, STEPHEN NIGEL
To: CHAVAH PTY LTD.
Reel/Frame 037366/0873 →
Priority Claims (1)
AU 2005905768 · Oct 19, 2005 · national
Continuity (5)
Continuation 13354103 · Jan 19, 2012
Continuation 12083771
Provisional Application 60798308 · May 8, 2006
Provisional Application 60732662 · Nov 3, 2005
Related Publication 20160129015A1 · May 12, 2016