IP Library Granted Patent US 7,208,178
Granted Patent B2
US 7,208,178 · App. 11/183,039 · Granted Apr 24, 2007

Polymorphs of sodium 4-[(4-chloro-2-hydroxybenzoyl) amino] butanoate

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Quick Facts
Patent No.
US 7,208,178
App. No.
11/183,039
Granted
Apr 24, 2007
Kind
B2
Abstract

The present invention relates to amorphous and polymorphic forms of sodium 4-[(4-chloro-2-hydroxybenzoyl)amino]butanoate and their use for facilitating the delivery of active agents, such as insulin, to a target.

Claims (38)

1. A crystalline polymorph of anhydrous sodium 4-[(4-chloro-2-hydroxybenzoyl)amino]butanoate exhibiting an X-ray powder diffraction pattern substantially as shown in FIG. 1 .

2. A crystalline polymorph of anhydrous sodium 4-[(4-chloro-2-hydroxybenzoyl)amino]butanoate exhibiting an X-ray powder diffraction pattern having peaks in degrees 2Θ±0.2° 2Θ at 5.2, 11.2, 15.7, 18.5, 20.1, 21.8, 23.4, 23.8, 26.9, and 29.8.

3. The crystalline polymorph of claim 2 , wherein the crystalline polymorph has a melting point onset as determined by differential scanning calorimetry at about 215.07° C.

4. A composition comprising

(a) a crystalline polymorph of any one of claims 1 – 3 ; and

(b) a biologically active agent.

5. The composition of claim 4 , wherein the biologically active agent comprises at least one protein, polypeptide, peptide, hormone, polysaccharide, mucopolysaccharide, small polar organic molecules, carbohydrate, or lipid.

6. The composition of claim 4 , wherein the biologically active agent is selected from the group consisting of growth hormones, human growth hormones (hGH), recombinant human growth hormones (rhGH), bovine growth hormones, porcine growth hormones, growth hormone-releasing hormones, interferons, α-interferon, β-interferon, γ-interferon, interleukin-1, interleukin-2, insulin, porcine insulin, bovine insulin, human insulin, human recombinant insulin, insulin-like growth factor(IGF), IGF-1, heparin, unfractionated heparin, heparinoids, dermatans, chondroitins, low molecular weight heparin, very low molecular weight heparin, ultra low molecular weight heparin, calcitonin, salmon calcitonin, eel calcitonin, human calcitonin, erythropoietin (EPO), atrial naturetic factor, antigens, monoclonal antibodies, somatostatin, protease inhibitors, adrenocorticotropin, gonadotropin releasing hormone, oxytocin, leutinizing-hormone-releasing-hormone, follicle stimulating hormone, glucocerebrosidase, thrombopoietin, filgrastim, prostaglandins, cyclosporin, vasopressin, cromolyn sodium, sodium chromoglycate, disodium chromoglycate, vancomycin, desferrioxamine, bisphosphonates, alendronate, tiludronate, etidronate, clodronate, pamidronate, olpadronate, incadronate, BIBN-4096BS, parathyroid hormone, fragments of parathyroid hormone, antimicrobials, daptomycin, anti-fungal agents, vitamins, analogs, fragments, mimetics and polyethylene glycol-modified derivatives of these compounds, and any combination thereof.

7. The composition of claim 6 , wherein the biologically active agent is insulin.

8. A dosage unit form comprising:

(A) the composition of claim 4 ; and

(B) (a) an excipient

(b) a diluent,

(c) a disintegrant,

(d) a lubricant,

(e) a plasticizer,

(f) a colorant,

(g) a dosing vehicle, or

(h) any combination thereof.

9. A dosage unit form comprising:

(A) the composition of claim 8 ; and

(B) (a) an excipient

(b) a diluent,

(c) a disintegrant,

(d) a lubricant,

(e) a plasticizer,

(f) a colorant,

(g) a dosing vehicle, or

(h) any combination thereof.

10. A method of administering an active agent to an animal in need thereof, the method comprising the step of administering the composition of claim 4 to the animal.

11. A method of treating diabetes in an animal in need thereof, comprising the step of administering a composition of claim 7 to the animal.

12. A method of treating diabetes in a human in need thereof, comprising the step of administering a composition of claim 7 to the human.

13. A method of preparing Form I of sodium 4-[(4-chloro-2-hydroxybenzoyl)amino]butanoate comprising the steps of:

(a) dissolving 4-[(4-chloro-2-hydroxybenzoyl)-amino]butanoic acid in an organic solvent to form a solution;

(b) adding a sodium source to the solution;

(c) heating the solution to reflux; and

(d) cooling the solution to yield Form I of sodium 4-[(4-chloro-2-hydroxybenzoyl)amino]butanoate.

14. A method of preparing Form I of sodium 4-[(4-chloro-2-hydroxybenzoyl)amino]butanoate comprising the step of heating Form II of sodium 4-[(4-chloro-2-hydroxybenzoyl)amino]butanoate, Form IV of sodium 4-[(4-chloro-2-hydroxybenzoyl)amino]butanoate, or a mixture thereof to above its solid state transition temperature.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 22, 2021
From: EMISPHERE TECHNOLOGIES, INC.
To: NOVO NORDISK NORTH AMERICA OPERATIONS A/S
Reel/Frame 056750/0169 →
SECURITY AGREEMENT Recorded Oct 3, 2005
From: EMISPHERE TECHNOLOGIES, INC.
To: MHR INSTITUTIONAL PARTNERS IIA LP
Reel/Frame 016617/0145 →