IP Library Patent Application 13238801
Patent Application
App. No. 13/238,801

CALCITONIN PRODUCTS AND THERAPIES FOR TREATING INFLAMMATORY OR DEGENERATIVE DISEASES

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Patent No.
US None
App. No.
13/238,801
Abstract

Calcitonin products and therapies for treating inflammatory or degenerative diseases are disclosed herein. The pharmaceutical compositions disclosed herein include a first therapeutic agent that is calcitonin, in free or salt form; a second therapeutic agent selected from the group consisting of a protease inhibitor, an antibiotic, a non-steroidal anti-inflammatory agent, a COX-2 inhibitor and a steroidal anti-inflammatory agent other than glucocorticoid; and a pharmaceutically acceptable excipient, carrier or diluent. The methods disclosed herein for treating inflammatory or degenerative diseases in a subject include administering a therapeutically effective amount of calcitonin, in free or salt form, to the subject; and co-administering, as part of a combination therapy, a therapeutically effective amount of a second therapeutic agent selected from the group consisting of a protease inhibitor, an antibiotic, a non-steroidal anti-inflammatory agent, a COX-2 inhibitor and a steroidal anti-inflammatory agent other than glucocorticoid to the subject.

Claims (27)

1 . A method for treating a degenerative or an inflammatory disease in a subject comprising:

administering a therapeutically effective amount of calcitonin, in free or salt form, to the subject; and

co-administering, as part of a combination therapy, a therapeutically effective amount of a matrix metalloproteinase inhibitor to the subject.

2 . The method of claim 1 wherein the calcitonin is selected from the group consisting of human calcitonin, salmon calcitonin, eel calcitonin and elcatonin.

3 . The method of claim 1 wherein the calcitonin is salmon calcitonin.

4 . The method of claim 1 wherein the matrix metalloproteinase inhibitor is selected from one of galardin or BB-94.

5 . The method of claim 1 wherein the calcitonin and the matrix metalloproteinase inhibitor are each administered to the subject orally.

6 . A method for treating a degenerative or an inflammatory disease in a subject comprising:

administering a therapeutically effective amount of calcitonin, in free or salt form, to the subject; and

co-administering, as part of a combination therapy, a therapeutically effective amount of a tetracycline antibiotic to the subject.

7 . The method of claim 6 wherein the calcitonin is selected from the group consisting of human calcitonin, salmon calcitonin, eel calcitonin and elcatonin.

8 . The method of claim 6 wherein the calcitonin is salmon calcitonin.

9 . The method of claim 6 wherein the tetracycline antibiotic is doxycycline.

10 . The method of claim 6 wherein the calcitonin and the tetracycline antibiotic are each administered to the subject orally.

11 . A pharmaceutical composition for the treatment of a degenerative or an inflammatory disease comprising:

a first therapeutic agent that is calcitonin, in free or salt form;

a second therapeutic agent selected from the group consisting of a matrix metalloproteases inhibitor, an interleukin antagonist, an aggrecanase inhibitor, a tetracyline antibiotic, and a COX-2 inhibitor; and

a pharmaceutically acceptable excipient, carrier or diluent.

12 . The pharmaceutical composition of claim 11 wherein the second therapeutic agent is a matrix metalloproteases inhibitor.

13 . The pharmaceutical composition of claim 11 wherein the second therapeutic agent is an interleukin antagonist.

14 . The pharmaceutical composition of claim 11 wherein the second therapeutic agent is an aggrecanase inhibitor.

15 . The pharmaceutical composition of claim 11 wherein the second therapeutic agent is a tetracyline antibiotic.

16 . The pharmaceutical composition of claim 11 wherein the second therapeutic agent is a COX-2 inhibitor.

17 . The pharmaceutical composition of claim 11 wherein the second therapeutic agent is administered at a dosage no higher than 90% of the normal dosage for the second therapeutic agent when administered alone.

18 . The pharmaceutical composition of claim 11 , wherein the composition is an aqueous nasal spray.

19 . The pharmaceutical composition of claim 11 , wherein the composition is a solid dosage form.

20 . The pharmaceutical composition of claim 11 wherein the calcitonin is salmon calcitonin.

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded Aug 8, 2019
From: VICTORY PARK MANAGEMENT, LLC
To: UNIGENE LABORATORIES, INC.
Reel/Frame 050000/0799 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2018
From: TARSA THERAPEUTICS, INC.
To: TAURUS DEVELOPMENT COMPANY LLC
Reel/Frame 047580/0917 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 22, 2016
From: UGP THERAPEUTICS, INC.
To: TARSA THERAPEUTICS, INC.
Reel/Frame 038350/0467 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 23, 2013
From: UNIGENE LABORATORIES, INC.
To: UGP THERAPEUTICS, INC.
Reel/Frame 030856/0340 →
SECURITY AGREEMENT Recorded Oct 4, 2012
From: UNIGENE LABORATORIES, INC.
To: VICTORY PARK MANAGEMENT, LLC, AS COLLATERAL AGENT
Reel/Frame 029074/0689 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 2, 2011
From: MEHTA, NOZER M.; GILLIGAN, JAMES P.
To: UNIGENE LABORATORIES INC.
Reel/Frame 027320/0585 →