IP Library Granted Patent US 10,231,982
Granted Patent B2
US 10,231,982 · App. 16/050,155 · Granted Mar 19, 2019

System and method for diagnosis and treatment

Inventors: Randice Lisa Altschul (Cliffside Park, NJ); Neil David Theise (New York, NY); Myron Rapkin (Indianapolis, IN); Rebecca O'Brien (Shell Knob, MO)
Assignee: Pop Test Oncology Limited Liability Company
A61K31/58A61J1/10A61K9/0019A61K9/08A61K9/10A61K9/107A61K31/337A61K38/09A61K45/06A61K47/10A61K47/26A61K47/34A61K47/42A61K47/44A61K51/00A61N5/1001B65D75/002B65D75/36B65D75/367C07J17/00G01N33/743G01N2333/575G01N2800/56
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,231,982
App. No.
16/050,155
Granted
Mar 19, 2019
Kind
B2
Abstract

This invention relates the use of cortisol blockers (glucocorticoid receptor [GR] antagonists) for the treating or preventing treatment resistant prostate cancer, treating or preventing neoplasia, and treating or preventing infection related to acute or chronic injury or disease.

Claims (17)

1. A pharmaceutical composition for treating or preventing infection related to acute or chronic injury or disease in a patient in need thereof, comprising:

(a) therapeutically effective amounts of at least one GCR (glucocorticoid receptor) antagonist selected from the group consisting of ORG 34517, 11-(substituted phenyl)-estra-4,9-diene derivatives, and 11-(substituted phenyl)-estra-4,9-diene derivatives of formula I

wherein A is a residue of a 5- or 6-membered ring containing 2 heteroatoms which are not connected to each other and independently selected from O and S, the ring being optionally substituted with one or more halogen atoms, or A is a residue of a 5- or 6-membered ring wherein no double C—C bonds are present, containing 1 heteroatom selected from O and S, which heteroatom is connected to the phenyl group at the position indicated with an asterisk, the ring being optionally substituted with one or more halogen atoms; R1 is H or 1-oxo(1-4C)alkyl; R2 is H, (1-8C)alkyl, halogen or CF3; X is selected from (H2OH), O, and NOH; and the interrupted line represents an optional bond, and combinations thereof; and

(b) optionally, at least one pharmaceutically acceptable carrier,

wherein the acute or chronic injury or disease is selected from the group consisting of vascular events, stroke, cardiac arrest, acute limb infraction accident/battle field trauma, traumatic limb, hip, brain injuries, post-surgical trauma, major orthopedic, thoracic, abdominal, neurological surgeries.

2. A kit for treating infection related to acute or chronic injury or disease comprising at least one blister package; a lidded blister; a blister card or packet; a clamshell; an intravenous (IV) package, IV packette or N container; a tray or a shrink wrap comprising the pharmaceutical composition of claim 1 , and instructions for use of the pharmaceutical composition for treating infection related to acute or chronic injury or disease.

3. A product of manufacture for treating infection related to acute or chronic injury or disease comprising a blister package; a lidded blister; a blister card or packet; a clamshell; an intravenous (IV) package, IV packette or IV container; a tray or a shrink wrap comprising a pharmaceutical composition comprising the pharmaceutical composition of claim 1 , and instructions for use of the pharmaceutical composition for treating infection related to acute or chronic injury or disease.

4. A method for treating or preventing infection related to acute or chronic injury or disease in a patient in need of such treatment, comprising:

administering to said animal or human therapeutically effective amounts of each of:

(a) therapeutically effective amounts of at least one GCR (glucocorticoid receptor) antagonist selected from the group consisting of ORG 34517, 11-(substituted phenyl)-estra-4,9-diene derivatives, and 11-(substituted phenyl)-estra-4,9-diene derivatives of formula I

wherein A is a residue of a 5- or 6-membered ring containing 2 heteroatoms which are not connected to each other and independently selected from O and S, the ring being optionally substituted with one or more halogen atoms, or A is a residue of a 5- or 6-membered ring wherein no double C—C bonds are present, containing 1 heteroatom selected from O and S, which heteroatom is connected to the phenyl group at the position indicated with an asterisk, the ring being optionally substituted with one or more halogen atoms; R1 is H or 1-oxo(1-4C)alkyl; R2 is H, (1-8C)alkyl, halogen or CF3; X is selected from (H2OH), O, and NOH; and the interrupted line represents an optional bond, and combinations thereof;

(b) optionally, at least one pharmaceutically acceptable carrier,

wherein the acute or chronic injury or disease is selected from the group consisting of vascular events, stroke, cardiac arrest, acute limb infraction accident/battle field trauma, traumatic limb, hip, brain injuries, post-surgical trauma, major orthopedic, thoracic, abdominal, neurological surgeries.

5. The method of claim 4 wherein the glucocorticoid receptor antagonist is selected from the group consisting of ORG 34517, 11-(substituted phenyl)-estra-4,9-diene derivatives, and 11-(substituted phenyl)-estra-4,9-diene derivatives of formula I

wherein A is a residue of a 5- or 6-membered ring containing 2 heteroatoms which are not connected to each other and independently selected from O and S, the ring being optionally substituted with one or more halogen atoms, or A is a residue of a 5- or 6-membered ring wherein no double C—C bonds are present, containing 1 heteroatom selected from O and S, which heteroatom is connected to the phenyl group at the position indicated with an asterisk, the ring being optionally substituted with one or more halogen atoms; R1 is H or 1-oxo(1-4C)alkyl; R2 is H, (1-8C)alkyl, halogen or CF3; X is selected from (H2OH), O, and NOH; and the interrupted line represents an optional bond, and combinations thereof.

6. The method of claim 4 wherein the at least one glucocorticoid receptor antagonist is in a pharmaceutical preparation.

7. A method for treating or preventing infection related to acute or chronic injury or disease in a patient in need of such treatment wherein said method comprises administering to a patient in need of such therapy at least one glucocorticoid receptor antagonist in a therapeutically effective amount, wherein the acute or chronic injury or disease is selected from the group consisting of vascular events, stroke, cardiac arrest, acute limb infraction accident/battle field trauma, traumatic limb, hip, brain injuries, post-surgical trauma, major orthopedic, thoracic, abdominal, neurological surgeries.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 9, 2018
From: ALTSCHUL, RANDICE LISA; THEISE, NEIL DAVID; RAPKIN, MYRON; OBRIEN, REBECCA
To: POP TEST ONCOLOGY LIMITED LIABILITY COMPANY
Reel/Frame 046599/0872 →
Continuity (12)
Division 15854053 · Dec 26, 2017
Division 15471123 · Mar 28, 2017
Division 15095293 · Apr 11, 2016
Division 14802060 · Jul 17, 2015
Continuation In Part 14100714 · Dec 9, 2013
Division 13364651 · Feb 2, 2012
Provisional Application 61462492 · Feb 3, 2011
Provisional Application 61463212 · Feb 14, 2011
Provisional Application 61465703 · Mar 23, 2011
Provisional Application 61518248 · May 3, 2011
Provisional Application 61519323 · May 20, 2011
Related Publication 20180360852A1 · Dec 20, 2018
Cited By (2)
US 12,383,543 US 12,734,180