IP Library › Granted Patent US 8,242,137
Granted Patent B2
US 8,242,137 · App. 12/563,727 · Granted Aug 14, 2012

Crystalline forms of a biphenyl compound

Assignee: Theravance, Inc.
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Quick Facts
Patent No.
US 8,242,137
App. No.
12/563,727
Granted
Aug 14, 2012
Kind
B2
Abstract

The invention provides crystalline forms of biphenyl-2-ylcarbamic acid 1-(2-{[4-(4-carbamoylpiperidin-1-ylmethyl)benzoyl]methylamino}ethyl)piperidin-4-yl ester, and pharmaceutically acceptable solvates thereof. The crystalline form can be a freebase, or a salt such as a diphosphate, monosulfate or dioxalate salt. The invention also provides pharmaceutical compositions comprising these crystalline compounds or prepared using these compounds; processes and intermediates for preparing the crystalline compounds; and methods of using these compounds to treat a pulmonary disorder.

Claims (14)

1. A pharmaceutical composition comprising a pharmaceutically acceptable carrier, about 6 weight percent of water, and a crystalline salt of biphenyl-2-ylcarbamic acid 1-(2-{[4-(4-carbamoylpiperidin-1-ylmethyl)benzoyl]methylamino}ethyl)piperidin-4-yl ester and phosphoric acid in a 1:2 molar ratio in a micronized form and characterized by a powder x-ray diffraction pattern comprising diffraction peaks at 2θ values of 15.0±0.2, 19.4±0.2, 21.6±0.2, and 23.7±0.2 and characterized by a differential scanning calorimetry trace which shows a maximum endothermic heat flow at about 154.5° C.

2. The composition of claim 1 , wherein the crystalline salt is characterized by a powder x-ray diffraction pattern further comprising two or more diffraction peaks at 2θ values selected from 6.4±0.2, 7.6±0.2, 8.6±0.2, 13.7±0.2, 22.1±0.2, and 22.9±0.2.

3. The composition of claim 1 , wherein the crystalline salt is characterized by a powder x-ray diffraction pattern in which the peak positions are substantially in accordance with the peak positions of the pattern shown in FIG. 1 .

4. The composition of claim 1 , wherein the crystalline salt is characterized by a differential scanning calorimetry trace substantially in accordance with that shown in FIG. 2 .

5. The composition of claim 1 , wherein the composition is formulated for administration by inhalation.

6. The composition of claim 1 , which is in the form of a powder.

7. The composition of claim 6 , wherein the crystalline salt is combined with the carrier to form a suspension.

8. The composition of claim 6 , wherein the crystalline salt is combined with the carrier to form a free flowing powder.

9. The composition of claim 8 , wherein the carrier is lactose or starch.

10. The composition of claim 6 , which is administered using a dry powder inhaler.

11. The composition of claim 1 , which is in the form of an aerosol.

12. The composition of claim 11 , which further comprises a liquefied propellant.

13. The composition of claim 11 , which is administered using a metered-dose inhaler.

14. The composition of claim 1 , which is administered using a nebulizer inhaler.

Assignments (2)
SECURITY INTEREST Recorded Sep 24, 2026
From: THERAVANCE BIOPHARMA R&D IP, LLC
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION
Reel/Frame 076134/0790 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 3, 2014
From: THERAVANCE, INC.
To: THERAVANCE BIOPHARMA R&D IP, LLC
Reel/Frame 033127/0174 →
Continuity (4)
Division 11890880 · Aug 8, 2007
Continuation 11371445 · Mar 9, 2006
Provisional Application 60660208 · Mar 10, 2005
Related Publication 20100021395A1 · Jan 28, 2010