生物活性 | |||
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描述 | Atosiban is a nonapeptide competitive vasopressin/oxytocin receptor antagonist, and is a desamino-oxytocin analogue. Atosiban inhibits the oxytocin-mediated release of IP3 from the myometrial cell membrane. There is reduced release of intracellular, stored calcium from the sacroplasmic reticulum of myometrial cells, and reduced influx of Ca2+ from the extracellular space through voltage gated channels. In addition, Atosiban suppresses oxytocin-mediated release of PGE and PGF from the decidua[3]. Atosiban resulted in fewer maternal side-effects than nifedipine, with no difference in pregnancy prolongation[4]. |
临床研究 | |||||
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NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
NCT00599898 | Labor, Premature | Phase 4 | Completed | - | Israel ... 展开 >> HaEmek Medical Center Afula, Israel, 18100 收起 << |
NCT01796522 | Preterm Delivery. | Phase 3 | Withdrawn(have been published ... 展开 >>new studies that it showed the ineffectiveness of the treatments proposed in this study.) 收起 << | May 2013 | Spain ... 展开 >> Hospital Universitari y Politécnic La Fe Valencia, Spain, 46026 收起 << |
NCT02292784 | Obstetric Labour, Premature | Phase 2 Phase 3 | Recruiting | July 29, 2022 | - |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.01mL 0.20mL 0.10mL |
5.03mL 1.01mL 0.50mL |
10.06mL 2.01mL 1.01mL |
参考文献 |
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