IP Library › Patent Application 12970013
Patent Application
App. No. 12/970,013

CRYSTALLINE FORMS OF A DIMETHYLPHENYL COMPOUND

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 None
App. No.
12/970,013
Abstract

The invention relates to crystalline free base forms of biphenyl-2-ylcarbamic acid 1-[2-(4-{[(R)-2-(3-formylamino-4-hydroxyphenyl)-2-hydroxyethylamino]methyl}-2,5-dimethylphenylcarbamoyl)ethyl]piperidin-4-yl ester or a solvate thereof. This invention also relates to pharmaceutical compositions containing or prepared from such crystalline forms; processes and intermediates useful for preparing such crystalline forms; and methods of using such crystalline forms to, for example, treat a pulmonary disorder.

Claims (12)

1 - 22 . (canceled)

23 . A method of treating chronic obstructive pulmonary disease or asthma, the method comprising administering to a patient a therapeutically effective amount of a crystalline free base form of biphenyl-2-ylcarbamic acid 1-[2-(4-{[(R)-2-(3-formylamino-4-hydroxyphenyl)-2-hydroxyethylamino]methyl}-2,5-dimethylphenylcarbamoyl)ethyl]piperidin-4-yl ester selected from:

(a) Form I characterized by a powder x-ray diffraction pattern having diffraction peaks at 2θ values of about 17.7±0.3, 18.2±0.3, 21.7±0.3 and 23.2±0.3;

(b) Form II characterized by a powder x-ray diffraction pattern having diffraction peaks at 2θ values of about 20.7±0.3, 21.6±0.3, 22.5±0.3 and 23.2±0.3; and

(c) Form III characterized by a powder x-ray diffraction pattern having diffraction peaks at 2θ values of about 15.5±0.3, 18.1±0.3, 19.2±0.3 and 21.8±0.3.

24 . A method of producing bronchodilation in a mammal, the method comprising administering to a mammal a bronchodilation-producing amount of a crystalline free base form of biphenyl-2-ylcarbamic acid 1-[2-(4-{[(R)-2-(3-formylamino-4-hydroxyphenyl)-2-hydroxyethylamino]methyl}-2,5-dimethylphenylcarbamoyl)ethyl]piperidin-4-yl ester selected from:

(a) Form I characterized by a powder x-ray diffraction pattern having diffraction peaks at 2θ values of about 17.7±0.3, 18.2±0.3, 21.7±0.3 and 23.2±0.3;

(b) Form II characterized by a powder x-ray diffraction pattern having diffraction peaks at 2θ values of about 20.7±0.3, 21.6±0.3, 22.5±0.3 and 23.2±0.3; and

(c) Form III characterized by a powder x-ray diffraction pattern having diffraction peaks at 2θ values of about 15.5±0.3, 18.1±0.3, 19.2±0.3 and 21.8±0.3.

25 - 27 . (canceled)

28 . The method of claim 23 or 24 , wherein the crystalline free base form 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 , FIG. 2 or FIG. 3 .

29 . The method of claim 23 or 24 , wherein the crystalline free base form is characterized by a differential scanning calorimetry trace which is substantially in accordance with that shown in FIG. 4 , FIG. 5 or FIG. 6 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 12, 2020
From: THERAVANCE RESPIRATORY COMPANY, LLC
To: THERAVANCE BIOPHARMA R&D IP, LLC
Reel/Frame 054393/0695 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 10, 2014
From: THERAVANCE, INC.
To: THERAVANCE RESPIRATORY COMPANY, LLC
Reel/Frame 033175/0620 →