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    • 5. 发明申请
    • DOSAGE FORM AND METHOD OF USE
    • 剂型及使用方法
    • US20090035370A1
    • 2009-02-05
    • US12183989
    • 2008-07-31
    • Jonathan David BortzMichael Norman Grimshaw
    • Jonathan David BortzMichael Norman Grimshaw
    • A61K9/52A61K31/554A61K9/22A61P25/00
    • A61K31/553
    • A method for treating a medical condition for which quetiapine is indicated in a subject comprises comprising orally administering to the subject quetiapine or a pharmaceutically acceptable salt thereof in a daily dosage amount effective to treat said condition; wherein the quetiapine or salt thereof is administered in one to a plurality of dosage forms collectively comprising (a) a major quetiapine component in immediate-release form in a sedative effective amount, administered not earlier than about 3 hours prior to the start of a sleep period; and (b) either (i) a minor quetiapine component in extended-release, delayed extended-release or delayed pulsed-release form, wherein time of administration and release properties of the minor component provide substantial onset of release of quetiapine therefrom not earlier than about 6 hours after the start of the sleep period, or (ii) a plurality of minor quetiapine components in immediate-release form, administered sequentially during a waking period following the sleep period but not earlier than about 6 hours after the start of the sleep period; said minor component or components collectively being administered in an anxiolytic effective amount insufficient to cause an unacceptable degree of sedation. A dosage form suitable for use in such a method is also provided.
    • 用于治疗在受试者中表示喹硫平的医学状况的方法包括以有效治疗所述病症的日剂量来口服给予受试者喹硫平或其药学上可接受的盐; 其中喹硫平或其盐以一种至多种剂型的形式一起给药,包括(a)一种镇静有效量的即时释放形式的主要喹硫平组分,其不早于睡眠开始前约3小时施用 期; (b)(i)延长释放,延迟释放或延迟脉冲释放形式中的次要喹硫平组分,其中次要组分的给药时间和释放特性提供了不迟于 在睡眠期开始约6小时后,或(ii)多个次要的喹硫平组分,其在睡眠期后醒后期间依次施用,但不迟于睡眠开始后约6小时 期; 所述次要成分或组分共同以抗焦虑有效量施用,不足以引起不可接受的镇静程度。 还提供了适合用于这种方法的剂型。
    • 9. 发明申请
    • COMPOSITIONS INCLUDING IRON
    • 包括铁的组成
    • US20090035385A1
    • 2009-02-05
    • US12195170
    • 2008-08-20
    • Jonathan David Bortz
    • Jonathan David Bortz
    • A61K33/42A61K33/26A61K31/295A61K38/16A61P3/02
    • A61K33/26A61K31/19A61K31/375Y02A50/411A61K2300/00
    • Compositions and methods for prevent, stabilize, reverse or treat disorders related to iron deficiency in a human or other animal. In a first embodiment, the composition includes about 10 mg to about 500 mg of one or more forms of iron, wherein at least one form of iron is an aspartic acid-glycine chelate of iron; and about 5 mg to about 500 mg of one or more forms of an organic acid. In another embodiment, the composition includes about 50 to about 150 mg of one or more forms of iron, wherein at least one form of iron is an aspartic acid-glycine chelate of iron; about 50 to about 250 mg of one or more forms of an organic acid; about 150 to about 250 mg of one or more forms of ascorbic acid; about 0.5 mg to about 1.5 mg vitamin B12; about 50 to about 150 mg intrinsic factor; and about 0.5 mg to about 1.5 mg folic acid.
    • 用于预防,稳定,逆转或治疗与人类或其他动物中的铁缺乏有关的疾病的组合物和方法。 在第一个实施方案中,组合物包含约10mg至约500mg的一种或多种形式的铁,其中至少一种形式的铁是铁的天冬氨酸 - 甘氨酸螯合物; 和约5mg至约500mg的一种或多种形式的有机酸。 在另一个实施方案中,组合物包含约50至约150mg的一种或多种形式的铁,其中至少一种形式的铁是铁的天冬氨酸 - 甘氨酸螯合物; 约50至约250mg的一种或多种形式的有机酸; 约150至约250mg的一种或多种形式的抗坏血酸; 约0.5mg至约1.5mg维生素B12; 约50至约150毫克内在因素; 和约0.5mg至约1.5mg叶酸。