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公开(公告)号:US20170251715A1
公开(公告)日:2017-09-07
申请号:US15062907
申请日:2016-03-07
Applicant: R.J. REYNOLDS TOBACCO COMPANY
Inventor: Serban C. Moldoveanu , Wayne Allen Scott
CPC classification number: A24B15/302 , A24B13/00 , A24B15/345 , A61K9/007 , A61K31/56 , A61K36/53 , A61K36/81 , A61K2300/00
Abstract: Provided are smoking products and methods of preparing smoking products that include tobacco and a deflavored rosemary or a heat-treated rosemary. The deflavored and/or heat-treated rosemary may have been previously heated at a temperature and a time sufficient to reduce or remove flavorant components compared to the use of untreated rosemary. The heated rosemary may include one or more pentacyclic triterpenoid acids such as betulinic, betul-18-enoic, oleanolic, and ursolic acids.
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公开(公告)号:US20170239269A1
公开(公告)日:2017-08-24
申请号:US15519460
申请日:2015-10-16
Inventor: Mukul Dalvi , Jacquelyn McCabe
CPC classification number: A61K31/56 , A61K9/0075 , A61K9/008 , A61K9/124
Abstract: This invention provides a process for preparing an inhalable active pharmaceutical ingredient comprising the steps of heating a suspension of an active pharmaceutical ingredient in a liquefied propellant in a vessel, evaporating the propellant and collecting the resultant powder.
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83.
公开(公告)号:US20170231967A1
公开(公告)日:2017-08-17
申请号:US15584459
申请日:2017-05-02
Applicant: vTv Therapeutics LLC
Inventor: Otis Clinton Attucks
IPC: A61K31/437 , A61K31/56 , A61K31/428
CPC classification number: A61K31/437 , A61K31/428 , A61K31/56 , Y02A50/395
Abstract: The disclosure provides pharmaceutical compositions comprising Bach1 Inhibitors and Nrf2 Activators. The disclosure also provides methods of treating diseases such as psoriasis, multiple sclerosis, and COPD comprising administering a Bach1 Inhibitor and a Nrf2 Activator to a subject in need thereof.
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84.
公开(公告)号:US09717743B2
公开(公告)日:2017-08-01
申请号:US14485335
申请日:2014-09-12
Applicant: Allergan, Inc.
Inventor: Jeffrey L. Edelman , Alissar Nehme
IPC: A61K31/56 , A61K31/575 , A61K31/58 , C07J7/00 , C07J17/00 , C07J31/00 , A61K9/00 , A61K31/573 , C07J5/00
CPC classification number: A61K31/58 , A61K9/0048 , A61K31/56 , A61K31/573 , A61K31/575 , A61K2121/00 , C07J5/0053 , C07J7/008 , C07J17/00 , C07J31/006
Abstract: The present invention relates to pharmaceutical compositions comprising 4-pregenen-11β-17-21-triol-3,20-dione derivatives, and their use as pharmaceuticals as modulators of the glucocorticoid receptors (GR) and/or the mineralocorticoid receptors (MR). The invention relates specifically to the use of these compounds and their pharmaceutical compositions to treat ocular conditions associated with the glucocorticoid receptors (GR) and/or the mineralocorticoid receptors (MR).
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公开(公告)号:US20170196985A1
公开(公告)日:2017-07-13
申请号:US15316742
申请日:2015-06-05
Applicant: THE SCRIPPS RESEARCH INSTITUTE
Inventor: Jiajia DONG , K. Barry SHARPLESS , Jeffery W. KELLY , Aleksandra BARANCZAK , Wentao CHEN
IPC: A61K47/48 , C07K1/02 , C07K2/00 , A61K31/56 , A61K31/5513 , A61K31/515 , A61K31/485 , A61K31/4353 , A61K31/65 , A61K31/7048 , A61K31/70 , A61K31/05 , A61K31/655 , A61K31/4245 , A61K31/407 , A61K31/4168 , A61K31/40 , A61K31/505 , A61K31/14 , A61K31/473 , A61K31/53 , A61K31/197 , A61K31/4745 , A61K31/47 , A61K31/397 , A61K31/198 , A61K38/31 , A61K31/439 , A61K31/4045 , A61K51/04 , A61K31/136 , A61K31/4709 , C07C305/26 , C07K1/113 , C07K19/00
CPC classification number: A61K31/05 , A61K31/136 , A61K31/14 , A61K31/197 , A61K31/198 , A61K31/397 , A61K31/40 , A61K31/4045 , A61K31/407 , A61K31/4168 , A61K31/4245 , A61K31/4353 , A61K31/439 , A61K31/47 , A61K31/4709 , A61K31/473 , A61K31/4745 , A61K31/485 , A61K31/505 , A61K31/515 , A61K31/53 , A61K31/5513 , A61K31/56 , A61K31/65 , A61K31/655 , A61K31/70 , A61K31/7048 , A61K38/31 , A61K47/54 , A61K51/0497 , C07C305/26 , C07C2601/14 , C07C2603/18 , C07D277/82 , C07D295/088 , C07D295/185 , C07D295/26 , C07K1/02 , C07K1/1136 , C07K2/00
Abstract: This application describes a compound represented by Formula (I): (I) wherein: Y is a biologically active organic core group comprising one or more of an aryl group, a heteroaryl aryl group, a nonaromatic hydrocarbyl group, and a nonaromatic heterocyclic group, to which Z is covalently bonded; n is 1, 2, 3, 4 or 5; m is 1 or 2; Z is O, NR, or N; X1 is a covalent bond or —CH2CH2—, X2 is O or NR; and R comprises H or a substituted or unsubstituted group selected from an aryl group, a heteroaryl aryl group, a nonaromatic hydrocarbyl group, and a nonaromatic heterocyclic group. Methods of preparing the compounds, methods of using the compounds, and pharmaceutical compositions comprising the compounds are described as well.
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公开(公告)号:US20170196935A1
公开(公告)日:2017-07-13
申请号:US15241895
申请日:2016-08-19
Applicant: CSL Limited
Inventor: Samuel Wright , Martin Imboden , Reinhard Bolli , Marcel Waelchli
IPC: A61K38/17 , A61K31/575 , A61K31/685
CPC classification number: A61K38/1709 , A61K9/0019 , A61K9/1275 , A61K31/56 , A61K31/575 , A61K31/685 , A61K45/06 , A61K2300/00
Abstract: A reconstituted high density lipoprotein formulation having relatively low toxicity comprises an apolipoprotein such as ApoAI or fragment thereof, a lipid and a detergent at a level which is about 5-50% of that which would normally cause liver toxicity upon administration to a human. The lipid is optimally phosphatidylcholine at about 30-50 g/L and the molar ratio of apolipoprotein:lipid is optimally in the range 1:40 to 1:75. The formulation is useful for treating diseases or conditions such as cardiovascular disease, hypercholesterolaemia and hypocholesterolaemia inclusive of acute coronary syndrome (ACS), atherosclerosis and myocardial infarction.
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公开(公告)号:US20170196823A1
公开(公告)日:2017-07-13
申请号:US14990168
申请日:2016-01-07
Applicant: CMPD LICENSING, LLC
Inventor: Jay Richard Ray, III
IPC: A61K31/17 , A61K31/496 , A61K47/10 , A61K9/06 , A61K9/00 , A61K31/56 , A61K31/351
CPC classification number: A61K31/17 , A61K9/0014 , A61K9/06 , A61K31/351 , A61K31/496 , A61K31/56 , A61K47/10 , A61K2300/00
Abstract: A topical cream may include urea and one or more additional active agents such as fluticasone, itraconazole, and mupirocin. The topical cream may be formulated as a lotion, gel, ointment, foam, cream, or emulsion
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公开(公告)号:US20170188902A1
公开(公告)日:2017-07-06
申请号:US15394650
申请日:2016-12-29
Applicant: DexCom, Inc.
Inventor: Shanger Wang , Ted Tang Lee , Jiong Zou
IPC: A61B5/1473 , C12Q1/00 , A61B5/145 , C12N11/08
CPC classification number: G01N27/3273 , A61B5/0004 , A61B5/002 , A61B5/14532 , A61B5/14546 , A61B5/1473 , A61B5/1486 , A61B5/14865 , A61B2562/12 , A61K31/045 , A61K31/137 , A61K31/46 , A61K31/465 , A61K31/485 , A61K31/515 , A61K31/56 , A61K33/00 , A61K36/185 , A61K38/28 , C08G18/0828 , C08G18/12 , C08G18/3857 , C08G18/4018 , C08G18/44 , C08G18/4833 , C08G18/755 , C08L39/06 , C08L69/00 , C08L75/04 , C12N11/08 , C12Q1/002 , C12Q1/006 , G01N27/3275 , G01N33/66 , C08G18/3234
Abstract: Disclosed are devices for determining an analyte concentration (e.g., glucose). The devices comprise a sensor configured to generate a signal associated with a concentration of an analyte and a sensing membrane located over the sensor. The sensing membrane comprises an enzyme layer, wherein the enzyme layer comprises an enzyme and a polymer comprising polyurethane and/or polyurea segments and one or more zwitterionic repeating units. The enzyme layer protects the enzyme and prevents it from leaching from the sensing membrane into a host or deactivating.
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公开(公告)号:US20170173048A1
公开(公告)日:2017-06-22
申请号:US15129539
申请日:2015-03-30
Applicant: Vesna Jevtovic-Todorovic , Slobodan Todorovic
Inventor: Vesna Jevtovic-Todorovic , Slobodan Todorovic
IPC: A61K31/568
CPC classification number: A61K31/568 , A61K31/56 , A61K31/565 , A61K31/58
Abstract: The present application discloses the unexpected result that a neuroactive steroid such as B260 can act as a general anesthetic and that it has no neurotoxic side effects such as impairing brain development.
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公开(公告)号:US20170172925A1
公开(公告)日:2017-06-22
申请号:US15453940
申请日:2017-03-09
Applicant: Norton Healthcare Ltd.
Inventor: Xian-Ming ZENG , Seah Kee TEE
IPC: A61K9/16 , A61K31/56 , A61K31/167 , A61K9/00 , A61K31/58
CPC classification number: A61K9/1623 , A61K9/0075 , A61K9/1694 , A61K31/137 , A61K31/167 , A61K31/56 , A61K31/58
Abstract: The present invention provides a process for preparing a particulate medicament that has greater homogeneity and a lower adhesion between the particles of the active ingredient and the carrier. The process comprises the steps of: (a) combining a pharmaceutically active ingredient in the form of an agglomerate of primary particles having an agglomerate particle size such that the agglomerate is capable of passing through a sieve having a mesh of 50-3000 .mu·m with a pharmaceutically acceptable particulate carrier, and (b) mixing the resultant material in a mixer to break up the agglomerate into primary particles dispersed in the pharmaceutically acceptable particulate carrier such that 90% or more of the pharmaceutically active ingredient exists as primary particles having a particle size of 50 .mu·m or less.
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