US2016022660A1PendingUtilityA1
Crystalline form of a 4-[2-(2-fluorophenoxymethyl)phenyl]piperidine compound
Est. expiryNov 14, 2028(~2.3 yrs left)· nominal 20-yr term from priority
A61P 9/00A61P 43/00A61P 9/02A61P 25/28A61P 25/08A61P 3/02A61P 25/16A61P 3/04A61P 25/04A61P 25/18A61P 29/00A61P 25/00A61P 25/14A61P 25/22A61P 25/30A61P 25/24A61P 3/00A61P 15/10A61P 19/02A61P 13/02A61P 13/10A61P 15/12A61P 13/00A61P 21/00A61P 11/06A61K 31/4465C07D 211/32C07D 211/22A61K 31/4409C07D 211/10A61K 31/451A61K 45/00
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Claims
Abstract
The invention provides a crystalline hydrochloride salt of 4-[2-(2,4,6-trifluorophenoxymethyl)phenyl]piperidine. This invention also provides pharmaceutical compositions comprising the crystalline salt, processes and intermediates for preparing the crystalline salt, and methods of using the crystalline salt to treat diseases.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 . The pharmaceutical composition of claim 7 , where the crystalline hydrochloride salt is characterized by having one or more additional diffraction peaks at 2θ values selected from 8.11±0.20, 13.18±0.20, 16.06±0.20, 18.38±0.20, 23.76±0.20, 26.32±0.20, 27.24±0.20, 29.60±0.20, and 31.94±0.20.
3 . The pharmaceutical composition of claim 7 , where the crystalline hydrochloride 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 pharmaceutical composition of claim 7 , where the crystalline hydrochloride salt is characterized by a differential scanning calorimetry trace which has a melting point of about 196.9° C.
5 . The pharmaceutical composition of claim 7 , where the crystalline hydrochloride salt is characterized by a differential scanning calorimetry trace substantially in accordance with that shown in FIG. 2 .
6 . (canceled)
7 . The pharmaceutical composition comprising a pharmaceutically acceptable carrier, crystalline hydrochloride salt of 4-[2-(2,4,6-trifluorophenoxymethyl)phenyl]-piperidine, characterized by a powder x-ray diffraction pattern comprising diffraction peaks at 2θ values of 4.44±0.20, 10.22±0.20, 17.16±0.20, and 21.78±0.20, and a secondary therapeutic agent selected from anticonvulsants, antidepressants, anti-Parkinson's agents, dual serotonin-norepinephrine reuptake inhibitors, non-steroidal anti-inflammatory agents, norepinephrine reuptake inhibitors, opioid agonists, opioid antagonists, selective serotonin reuptake inhibitors, sodium channel blockers, sympatholytics, and combinations thereof.
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