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    • 1. 发明申请
    • ENDOXIFEN METHODS AND COMPOSITIONS
    • ENDOXIFEN方法和组合物
    • WO2008070463A9
    • 2008-09-18
    • PCT/US2007085443
    • 2007-11-21
    • JINA PHARMACEUTICALS INCAHMAD ATEEQALI SHOUKATH MAHMAD MOGHIS USHEIKH SAIFUDDINAHMAD IMRAN
    • AHMAD ATEEQALI SHOUKATH MAHMAD MOGHIS USHEIKH SAIFUDDINAHMAD IMRAN
    • A61K31/35
    • A61K31/138A61K9/0014A61K9/127A61K9/19A61K31/35C07D309/10
    • The present invention provides compositions containing endoxifen, formulations and liposomes of endoxifen, methods of preparation of such agents and formulations, and use of such agents and formulations for the treatment of breast cancer and other breast diseases and diseases susceptible to endoxifen. In particular, the compositions of the present invention include liposomes, complexes, vesicles, emulsions, micelles and mixed micelles of endoxifen in which the compositions further contain any of a variety of neutral or charged lipids and desirably, cholesterol and cholesterol derivatives, sterols, Z- and E- guggulsterones, phospholipids, fatty acids, vitamin D, and vitamin E. The present invention also provides methods of preparing endoxifen. The present invention provides methods for treating and preventing breast cancer and other breast related diseases by administrating novel formulations or compositions comprising a therapeutically effective amount of endoxifen.
    • 本发明提供了包含endoxifen,endoxifen的制剂和脂质体的组合物,制备这些制剂和制剂的方法,以及这些制剂和制剂用于治疗乳腺癌和其他乳腺疾病和易患endoxifen的疾病的用途。 特别地,本发明的组合物包括endoxifen的脂质体,复合物,囊泡,乳剂,胶束和混合胶束,其中所述组合物进一步含有多种中性或带电脂质中的任何一种,并且期望胆固醇和胆固醇衍生物,甾醇,Z - 和E-胍酯,磷脂,脂肪酸,维生素D和维生素E.本发明还提供了制备烯诺昔芬的方法。 本发明提供了通过施用包含治疗有效量的多昔多芬的新制剂或组合物来治疗和预防乳腺癌和其他乳房相关疾病的方法。
    • 3. 发明申请
    • GUGGULPHOSPHOLIPID METHODS AND COMPOSITIONS
    • GUGGPHPHPHPHIPIPI方法和组合物
    • WO2008058156A2
    • 2008-05-15
    • PCT/US2007083832
    • 2007-11-06
    • JINA PHARMACEUTICALS INCAHMAD MOGHIS UALI SHOUKATH MAHMAD ATEEQSHEIKH SAIFUDDINAHMAD IMRAN
    • AHMAD MOGHIS UALI SHOUKATH MAHMAD ATEEQSHEIKH SAIFUDDINAHMAD IMRAN
    • A01N65/00
    • C07J13/007A61K31/337A61K47/554A61K47/6907A61K47/6911C07J7/0005C07J31/006C07J41/0005C07J41/0088C07J51/00C12N15/85
    • The present invention relates to the methods for preparing synthetic guggulphospholipids, their fatty acid analogues and other bioactive molecules. The present invention relates to E-guggulsterone and Z-guggulsterone or mixture of E- and Z-guggulsterones; and E-guggulsterol and Z-guggulsterol or mixture of E- and Z-guggulsterols synthetically modified to guggulphospholipids and analogues and salts thereof, fatty acid analogues of guggulsterols, guggulsulfate and salts thereof, guggulphosphate and salts thereof; and guggulsterols conjugated with drugs for use as prodrugs. Also the present invention provides a novel method for the preparation of E-guggulsterol and Z-guggulsterol or mixture of E-and Z-guggulsterols from a mixture of E- and Z-guggulsterones. The present invention further relates to guggulphospholipids and other bioactive molecules incorporated into complexes such as liposomes, complexes, emulsions, vesicles, micelles, and mixed micelles, which can include other active agents, such as hydrophobic or hydrophilic drugs for use, e.g., in treatment of human and animal diseases.
    • 本发明涉及制备合成瓜瓜磷脂,其脂肪酸类似物和其它生物活性分子的方法。 本发明涉及戊二酮和Z-鬼臼酮或E-和Z-格鲁酮的混合物; 合成修饰成瓜瓜尔斯醇和Z-guggulsterol或者合成修饰成瓜瓜尔斯醇及其类似物及其盐的瓜尔豆甾醇和Z-瓜格尔斯醇的混合物,瓜焦糖醇,巨硫酸盐及其盐的脂肪酸类似物,磷酸瓜瓜酯及其盐; 和与药物缀合的糖苷醇用作前药。 本发明还提供了一种从E-和Z-格鲁酮的混合物制备E-guggulsterol和Z-guggulsterol或E-和Z-苦瓜甾醇的混合物的新方法。 本发明还涉及结合到诸如脂质体,复合物,乳液,囊泡,胶束和混合胶束的复合物中的瓜瓜磷脂和其它生物活性分子,其可以包括其它活性剂,例如用于治疗的疏水或亲水药物 的人类和动物疾病。
    • 8. 发明申请
    • LIPID BASED PHARMACEUTICAL PREPARATIONS FOR ORAL AND TOPICAL APPLICATION; THEIR COMPOSITIONS, METHODS, AND USES THEREOF
    • 口服和局部应用的基于脂质的药物制剂; 其组合物,方法和用途
    • WO2010036947A2
    • 2010-04-01
    • PCT/US2009058463
    • 2009-09-25
    • ALI SHOUKATH MAHAMD ATEEQAHMAD MOGHIS USHEIKH SAIFUDDINAHMAD IMRANJINA PHARMACEUTICALS INC
    • ALI SHOUKATH MAHAMD ATEEQAHMAD MOGHIS USHEIKH SAIFUDDINAHMAD IMRAN
    • A61K47/44A61K31/506A61K31/58A61P17/14
    • A61K47/24A61K9/0014A61K9/08A61K9/10A61K31/506A61K31/58A61K45/06A61K47/44A61K2300/00
    • The present invention relates to the topical and oral delivery of a composition comprising one or more active agents for treating a disease or symptoms in a subject. In some embodiments, the present invention comprises a composition comprising at least one active compound, e.g., finasteride or minoxidil, and one or more lipids. In some embodiments, the present invention relates to composition and method of preparation for treating androgenic alopecia (AGA), prevention of hair loss and female hirsutism. In some embodiment, the present invention comprises finasteride and at least one lipid component for the treatment of benign prostatic hyperplasia. In some embodiment, the present invention comprises tacrolimus or amphotericin B and at least one lipid component for the treatment of skin or eye related diseases. The present invention provides a method of preparation of a composition comprising at least one active compound and at least one lipid and administering the composition to a subject by oral or topical delivery. In certain embodiments the subject is a mammal. In certain preferred embodiment, the subject is human.
    • 本发明涉及包含一种或多种用于治疗受试者中的一种或多种疾病的活性剂的组合物的局部和经口递送。 在一些实施方案中,本发明包含含有至少一种活性化合物,例如非那甾胺或米诺地尔和一种或多种脂质的组合物。 在一些实施方案中,本发明涉及用于治疗雄激素性脱发(AGA),预防脱发和女性多毛症的组合物和制备方法。 在一些实施方案中,本发明包含非那雄胺和至少一种用于治疗良性前列腺增生的脂质组分。 在一些实施方案中,本发明包含他克莫司或两性霉素B和至少一种用于治疗皮肤或眼睛相关疾病的脂质组分。 本发明提供了制备包含至少一种活性化合物和至少一种脂质的组合物的方法,并通过口服或局部递送将该组合物施用于受试者。 在某些实施方案中,受试者是哺乳动物。 在某些优选的实施方式中,所述对象是人。