IP Library Patent Application 16479063
Patent Application
App. No. 16/479,063

MACROCYCLIC PEPTIDES TO DECREASE C-MYC PROTEIN LEVELS AND REDUCE CANCER CELL GROWTH

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Quick Facts
Patent No.
US None
App. No.
16/479,063
Abstract

The present technology provides methods and medicaments useful for treating prostate cancer and breast cancer. Such methods include administering at least one of cyclo[Phe-D-Pro-Phe-Trp] and cyclo[Phe-D-Pro-Phe-D-Trp] to a subject suffering from prostate cancer or breast cancer.

Claims (22)

1 . A method comprising administering at least one of cyclo[Phe-D-Pro-Phe-Trp] and cyclo[Phe-D-Pro-Phe-D-Trp] or a pharmaceutically acceptable salt thereof to a subject suffering from prostate cancer or breast cancer.

2 . The method of claim 1 , wherein the method comprises administering an effective amount of at least one of cyclo[Phe-D-Pro-Phe-Trp] and cyclo[Phe-D-Pro-Phe-D-Trp] or a pharmaceutically acceptable salt thereof to the subject, wherein the effective amount is effective in treating the prostate cancer or the breast cancer.

3 . The method of claim 1 , wherein the prostate cancer comprises at least one oncogenic mutation found in a PC-3 cell line, a LNCaP cell line, a 22Rv1 cell line, a DU145 cell line, or a combination of any two or more thereof.

4 . The method of claim 1 , wherein the breast cancer comprises triple negative breast cancer.

5 . The method of claim 1 , wherein the breast cancer comprises at least one oncogenic mutation found in a BT-20 cell line, a MDA-MB-468 cell line, a MDA-MB-231 cell line, a MCF-7 cell line, a SKBR-3 cell line, a BT-474 cell ine, or a combination of any two or more thereof.

6 . The method of claim 1 , wherein administering comprises oral administration or parenteral administration.

7 . The method of claim 1 , wherein administering comprises at least one of subcutaneous administration, intravenous administration, and oral administration.

8 . The method of claim 1 , wherein the method comprises administering cyclo[Phe-D-Pro-Phe-Trp] or a pharmaceutically acceptable salt thereof.

9 . The method of claim 1 , wherein the method comprises administering cyclo[Phe-D-Pro-Phe-D-Trp] or a pharmaceutically acceptable salt thereof.

10 . The method of claim 1 , wherein the method comprises administering a composition comprising at least one of cyclo[Phe-D-Pro-Phe-Trp] and cyclo[Phe-D-Pro-Phe-D-Trp] and a pharmaceutically acceptable carrier.

11 . The method of claim 10 , wherein the composition is formulated for oral administration or parenteral administration.

12 . The method of claim 10 , wherein the composition is formulated for at least one of subcutaneous administration and intravenous administration.

13 . The method of claim 10 , wherein the pharmaceutically acceptable carrier comprises saline.

14 . The method of claim 10 , wherein the pharmaceutically acceptable carrier comprises polyethylene glycol, a polyethylene glycol fatty acid monoester, a polyethoxylene sorbitan ester, or a combination of any two or more thereof.

15 . The method of claim 10 , wherein the composition is a liquid formulation comprising about 0.1 mg/mL to about 50 mg/mL of the at least one of cyclo[Phe-D-Pro-Phe-Trp] and cyclo[Phe-D-Pro-Phe-D-Trp] or a pharmaceutically acceptable salt thereof.

16 . (canceled)

17 . The method of claim 1 , wherein the method comprises administering to the subject about 1 mg to about 150 mg of the at least one of cyclo[Phe-D-Pro-Phe-Trp] and cyclo [Phe-D-Pro-Phe-D-Trp] per kilogram of the subject.

18 . The method of claim 1 , wherein the method comprises administering to the subject from about 1 to about 7 times per week.

19 .- 22 . (canceled)

23 . The method of claim 2 , wherein the prostate cancer comprises at least one oncogenic mutation found in a PC-3 cell line, a LNCaP cell line, a 22Rv1 cell line, a DU145 cell line, or a combination of any two or more thereof.

24 . The method of claim 2 , wherein the breast cancer comprises triple negative breast cancer.

25 . The method of claim 2 , wherein the breast cancer comprises at least one oncogenic mutation found in a BT-20 cell line, a MDA-MB-468 cell line, a MDA-MB-231 cell line, a MCF-7 cell line, a SKBR-3 cell line, a BT-474 cell ine, or a combination of any two or more thereof.

Assignments (6)
CONFIRMATORY LICENSE Recorded Apr 26, 2022
From: UNIVERSITY OF KANSAS LAWRENCE
To: UNITED STATES GOVERNMENT
Reel/Frame 059791/0646 →
CONFIRMATORY LICENSE Recorded Apr 7, 2022
From: UNIVERSITY OF KANSAS LAWRENCE
To: UNITED STATES GOVERNMENT
Reel/Frame 059629/0484 →
CONFIRMATORY LICENSE Recorded Mar 31, 2022
From: UNIVERSITY OF KANSAS LAWRENCE
To: UNITED STATES GOVERNMENT
Reel/Frame 059558/0121 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 18, 2021
From: UNIVERSITY OF FLORIDA
To: UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INC.
Reel/Frame 058156/0964 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 30, 2019
From: ALDRICH, JANE; MUKHOPADHYAY, ARCHANA
To: UNIVERSITY OF KANSAS
Reel/Frame 050559/0278 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 30, 2019
From: HANOLD, LAURA E.
To: UNIVERSITY OF FLORIDA
Reel/Frame 050560/0227 →