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    • 31. 发明申请
    • METHOD AND APPARATUS FOR DIAGNOSING ERECTILE DYSFUNCTION
    • 用于诊断溃疡性功能障碍的方法和装置
    • WO1995026158A1
    • 1995-10-05
    • PCT/US1995003514
    • 1995-03-20
    • VIVUS, INC.
    • VIVUS, INC.PLACE, Virgil, A.
    • A61B05/00
    • A61B5/4393A61F5/41A61K9/0034A61M31/00
    • A method for diagnosing vasculogenic erectile dysfunction, including vasculogenic impotence and Peyronie's syndrome, is provided. The method involves transurethral administration of a vasodilating agent to induce an erection, followed by hemodynamic evaluation using duplex ultrasonography, NMR, angiography, or the like. Kits for conducting the diagnostic method are provided as well, as are methods of treatment based on the diagnostic conclusion. The kits for diagnosing erectile dysfunction comprise a vasodilating agent (4) effective to induce erection of the penis, a drug delivery means (1, 11, or 49) for administering the vasodilating agent transurethrally, a container (15 or 55) for housing the agent and drug delivery means, and written instructions for using the agent and the drug delivery means.
    • 提供了一种诊断血管性勃起功能障碍,包括血管性勃起功能障碍和佩罗尼氏综合征的方法。 该方法包括经尿道给药血管舒张剂诱导勃起,然后使用双相超声检查,NMR,血管造影术等进行血液动力学评估。 还提供了用于进行诊断方法的试剂盒,以及基于诊断结论的治疗方法。 用于诊断勃起功能障碍的试剂盒包括有效诱导勃起阴茎的血管扩张剂(4),用于经尿道施用血管舒张剂的药物递送装置(1,11或49),用于容纳阴茎的容器(15或55) 药剂和药物递送手段,以及使用该药剂和药物递送装置的书面说明。
    • 32. 发明申请
    • ORALLY DISINTEGRATING DOSAGE FORM FOR ADMINISTRATION OF AVANAFIL, AND ASSOCIATED METHODS OF MANUFACTURE AND USE
    • ORA用于治疗AVANAFIL的剂型及相关制造和使用方法
    • WO2015176008A1
    • 2015-11-19
    • PCT/US2015/031198
    • 2015-05-15
    • VIVUS, INC.
    • BROMAN, Calvin TheodoreSHEU, Eric
    • A61K9/00A61K9/20
    • A61K9/2031A61K9/0056A61K9/2018A61K9/2095A61K31/506
    • Formulations are provided for the oral administration of avanafil, a Type V phosphodiesterase inhibitor ("PDE V inhibitor"), and analogs thereof. The formulations are orally disintegrating tablets (ODTs) that rapidly dissolve or disintegrate in the oral cavity. The tablets contain an absorption enhancing composition that increases the duodenal absorption of the active agent, following transfer from the low pH environment of the stomach to the more basic pH of the duodenum. Methods for administering the active agent using the dosage forms are provided. The invention also encompasses a method of selecting components and compositions to incorporate in the formulations which will facilitate increased absorption of the active agent in the duodenum and thus serve as "absorption enhancing compositions" herein. Also provided are methods for manufacturing orally disintegrating tablets to optimize the physical properties of the dosage forms, particularly hardness and disintegration time.
    • 提供了用于口服给予阿伐他非,V型磷酸二酯酶抑制剂(“PDE V抑制剂”)及其类似物的制剂。 制剂是在口腔中快速溶解或分解的口腔崩解片(ODT)。 在从胃的低pH环境转移到十二指肠的更基本的pH之后,片剂含有增加活性剂的十二指肠吸收的吸收促进组合物。 提供了使用剂型给药活性剂的方法。 本发明还包括选择组合物和组合物以掺入制剂中的方法,其将促进活性剂在十二指肠中的增加的吸收,因此用作本文的“吸收增强组合物”。 还提供了制备口腔崩解片以优化剂型的物理性质,特别是硬度和崩解时间的方法。