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    • 9. 发明申请
    • IDENTIFYING PATIENT RESPONSE TO S1P RECEPTOR MODULATOR ADMINISTRATION
    • 鉴定患者对S1P受体调节剂的作用
    • WO2014161606A1
    • 2014-10-09
    • PCT/EP2013/058226
    • 2013-04-19
    • NOVARTIS AGBORELL, HubertGARDIN, AnneJIN, YiLEGANGNEUX, EricUFER, Mike
    • BORELL, HubertGARDIN, AnneJIN, YiLEGANGNEUX, EricUFER, Mike
    • G01N33/50C12Q1/68G01N33/569
    • C07D205/04C12Q1/6883C12Q2600/106C12Q2600/156G01N33/5094G01N33/56972G01N2800/52
    • The invention provides a method of assessing the appropriate therapeutic dose of 1-{4- [1-(4-cyclohexyl-3-trifluoromethyl-benzyloxyimino)-ethyl]-2-ethyl-benzyl}-azetidine-3- carboxylic acid to administer to a patient in need thereof, comprising the steps of: (i) testing whether or not the patient has the poor metabolizer genotype; and (ii) if the patient does not have the poor metaboliser genotype, administering -{4-[1-(4-cyclohexyl-3-trifluoromethyl-benzyloxyimino)-ethyl]-2-ethyl- benzyl}-azetidine-3-carboxylic acid, or a pharmaceutically acceptable salt thereof, to the patient at the standard therapeutic dose; and (iii) if the patient does have the poor metaboliser genotype, either (a) administering 1-{4-[1-(4-cyclohexyl-3-trifluoromethyl-benzyloxyimino)- ethyl]-2-ethyl-benzyl}-azetidine-3-carboxylic acid, or a pharmaceutically acceptable salt thereof, to the patient at a therapeutic dose below that of the standard therapeutic dose; or (b) not administering 1-{4-[1-(4-cyclohexyl-3-trifluoromethyl- benzyloxyimino)-ethyl]-2-ethyl-benzyl}-azetidine-3-carboxylic acid, or a pharmaceutically acceptable salt thereof, to the patient.
    • 本发明提供了评估1- {4- [1-(4-环己基-3-三氟甲基 - 苄氧基亚氨基) - 乙基] -2-乙基 - 苄基} - 氮杂环丁烷-3-羧酸的合适治疗剂量的方法, 包括以下步骤:(i)测试患者是否具有不良代谢基因型; 给予 - {4- [1-(4-环己基-3-三氟甲基 - 苄氧基亚氨基) - 乙基] -2-乙基 - 苄基} - 氮杂环丁烷-3-羧酸,并且(ii)如果患者不具有差的代谢基因型, 酸或其药学上可接受的盐以标准治疗剂量给予患者; (iii)如果患者确实具有差的代谢基因型,则(a)给予1- {4- [1-(4-环己基-3-三氟甲基 - 苄氧亚氨基) - 乙基] -2-乙基 - 苄基} - 氮杂环丁烷 -3-羧酸或其药学上可接受的盐以低于标准治疗剂量的治疗剂量给予患者; 或(b)不给予1- {4- [1-(4-环己基-3-三氟甲基 - 苄氧基亚氨基) - 乙基] -2-乙基 - 苄基} - 氮杂环丁烷-3-羧酸或其药学上可接受的盐, 给病人
    • 10. 发明申请
    • METHOD / DEVICE FOR GENERATING A CORRECTED VALUE OF AN ANALYTE CONCENTRATION IN A SAMPLE OF A BODY FLUID
    • 用于生成体液中样品分析浓度校正值的方法/装置
    • WO2014147074A1
    • 2014-09-25
    • PCT/EP2014/055418
    • 2014-03-18
    • ROCHE DIAGNOSTICS GMBHF. HOFFMANN-LA ROCHE AGHOENES, JoachimRINGEMANN, ChristianWELLER, Andreas
    • HOENES, JoachimRINGEMANN, ChristianWELLER, Andreas
    • G01N33/543
    • G01N33/5094G01N21/75G01N27/3272G01N27/3274G01N33/525G01N33/558G01N33/66
    • A method for detecting an analyte in a body fluid is disclosed. The method has the following steps: a) applying a sample (122) of the body fluid to a test element (120), said test element (120) comprising at least (i) a test field (128) comprising at least one test material (130) adapted to change at least one measurable property in the presence of the analyte, (ii) a capillary element (126) adapted to guide the sample (122) across said test field (128) in a flow direction (146), (iii) a first and a second measurement location (158, 160) within said test field (128), wherein the second measurement location (160) is offset from the first measurement location (158) in the flow direction (146); b) measuring the measurable property in said at least one first measurement location (158), thereby generating at least one first measurement value; c) measuring the measurable property in said at least one second measurement location (160), thereby generating at least one second measurement value; d) detecting the analyte by using an evaluation algorithm having at least two input variables, wherein (i) at least one first input variable of the at least two input variables includes an information on a difference between the first measurement value and the second measurement value, and (ii) at least one second input variable of the at least two input variables includes a measurement information on an analyte-induced change of the measurable property of the test material (130) in at least part of the test field (128).
    • 公开了一种用于检测体液中的分析物的方法。 该方法具有以下步骤:a)将体液样品(122)施加到测试元件(120),所述测试元件(120)包括至少(i)包括至少一个测试的测试场(128) 适于在存在分析物的情况下改变至少一个可测量性质的材料(130),(ii)适于在流动方向(146)上跨越所述测试场(128)引导样品(122)的毛细管元件(126) ,(iii)所述测试场(128)内的第一和第二测量位置(158,160),其中所述第二测量位置(160)在所述流动方向(146)上偏离所述第一测量位置(158); b)测量所述至少一个第一测量位置(158)中的可测量特性,由此产生至少一个第一测量值; c)测量所述至少一个第二测量位置(160)中的可测量特性,由此产生至少一个第二测量值; d)通过使用具有至少两个输入变量的评估算法来检测分析物,其中(i)至少两个输入变量的至少一个第一输入变量包括关于第一测量值和第二测量值之间的差的信息 ,和(ii)所述至少两个输入变量的至少一个第二输入变量包括关于在所述测试场(128)的至少一部分中所述测试材料(130)的可测量特性的分析物引起的变化的测量信息, 。