IP Library › Granted Patent US 10,512,667
Granted Patent B2
US 10,512,667 · App. 16/020,457 · Granted Dec 24, 2019

Compositions and methods for treating conditions related to adrenocortical activity and/or excessive steroid production

Inventors: Tom K. Kerppola (Ann Arbor, MI); Veronica E. Burns (Ann Arbor, MI)
Assignee: THE REGENTS OF THE UNIVERSITY OF MICHIGAN
A61K38/12A61K31/17A61K31/277A61K31/352A61K31/4725A61K31/496A61K31/4965A61K31/5685A61K31/64A61K38/13A61K45/06A61P5/42A61P5/46A61P35/00A61K31/18A61K35/04A61K2300/00
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Quick Facts
Patent No.
US 10,512,667
App. No.
16/020,457
Granted
Dec 24, 2019
Kind
B2
Abstract

Provided herein are methods for treating subjects having conditions related to adrenocortical activity and/or excessive steroid production. In particular, provided herein are methods for treating subjects having conditions related to adrenocortical activity and/or excessive steroid production through administration of at least one of the following agents: 1) an agent capable of inhibiting cholesterol efflux related to ABCA1 and/or ABCG1; 2) an agent capable of inhibiting MDR1 related cortisol secretion and/or MDR1 P-glycoprotein multiple drug transporter activity; and 3) an agent capable of inhibiting mitochondrial activity.

Claims (10)

1. A method of treating or ameliorating adrenocortical cancer comprising co-administering to said patient a therapeutically effective amount of two or more agents selected from

1) an agent capable of inhibiting cholesterol efflux related to ABCA1 and/or ABCG1;

2) an agent capable of inhibiting MDR1 related cortisol secretion and/or MDR1 P-glycoprotein multiple drug transporter activity; and

3) an agent capable of inhibiting mitochondrial activity, and

further comprising administering to said patient one or more anticancer agents, wherein said anticancer agent is a chemotherapeutic agent and/or radiation therapy.

2. The method of claim 1 ,

wherein the agent capable of inhibiting cholesterol efflux related to ABCA1 and/or ABCG1 is selected from Valspodar, Glyburide, Cyclosporine A,

wherein the agent capable of inhibiting MDR1 related cortisol secretion and/or MDR1 P-glycoprotein multiple drug transporter activity is selected from Tariquidar, MK-571, Niguldipine hydrochloride, Matairesinol, Reversin 121 (C 34 H 47 N 3 O 9 ), Elacridar, Pyrimethamine (C 12 H 13 ClN 4 ), Pyrimethamine Biotin (C 27 H 39 N 7 O 3 S), Pyrimethamine-d3 (C 12 H 10 D 3 ClN 4 ), 8-isopentenylnaringenin, JS-2190 (Boc-Glu(OBzl)-N,N′-dicyclohexylurea, C 30 H 45 N 3 O 6 ), P-Glycoprotein Inhibitor C-4 (C 23 H 18 ClNO 4 ), PGP-4008, Sipholenol A, Reversan, CP 100356 hydrochloride, PSC 833, Zosuquidar trihydrochloride, and Vismodegib,

wherein the agent capable of inhibiting mitochondrial activity is selected from rhodamine-123, MKT-077, decoquinate, isoniazid, suramin, erythrosine, toltrazuril, enilconazole, and metformin.

3. The method of claim 1 , wherein said patient is a human patient.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2019
From: KERPPOLA, TOM K.; BURNS, VERONICA E.
To: THE REGENTS OF THE UNIVERSITY OF MICHIGAN
Reel/Frame 048986/0107 →
Continuity (2)
Provisional Application 62525529 · Jun 27, 2017
Related Publication 20180369321A1 · Dec 27, 2018
Cited By (1)
US 12,377,096