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临床试验/NCT04290390
NCT04290390已完成1 期

A Drug-Drug Interaction Study to Evaluate the Effects of Strong CYP3A Induction and Inhibition on the Pharmacokinetics of Segesterone Acetate and Ethinyl Estradiol From the Annovera™ Contraceptive Vaginal System

TherapeuticsMD1 个研究点 分布在 1 个国家目标入组 67 人开始时间: 2020年2月12日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
67
试验地点
1
主要终点
Area-under-the-curve (AUC) of rifampin and itraconzaole on Annovera (segesterone acetate and ethinyl estradiol)

研究概览

简要总结

A Drug-Drug Interaction (DDI) study to evaluate the effects of itraconazole and rifampin on the Pharmacokinetics of Segesterone Acetate and Ethinyl Estradiol from the Annovera Contraceptive Vaginal System (CVS)

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Annovera with itraconazole use

Active Comparator

Subjects will dose with 200 mg/day of itraconazole for five days before Annovera insertion and through Days 1 to 8 of Annovera use

干预措施: Itraconazole (Drug)

Annovera (alone)

Active Comparator

Annovera taken alone (without itraconazole or rifampin)

干预措施: Segesterone Acetate and Ethinyl Estradiol (Drug)

Annovera with itraconazole use

Active Comparator

Subjects will dose with 200 mg/day of itraconazole for five days before Annovera insertion and through Days 1 to 8 of Annovera use

干预措施: Segesterone Acetate and Ethinyl Estradiol (Drug)

Annovera with rifampin use

Active Comparator

Subjects will dose with 600 mg/day rifampin for 8 days, between Days 4 to 11 of Annovera use during their respective treatment cycles

干预措施: Segesterone Acetate and Ethinyl Estradiol (Drug)

Annovera with rifampin use

Active Comparator

Subjects will dose with 600 mg/day rifampin for 8 days, between Days 4 to 11 of Annovera use during their respective treatment cycles

干预措施: Rifampin (Drug)

结局指标

主要结局

Area-under-the-curve (AUC) of rifampin and itraconzaole on Annovera (segesterone acetate and ethinyl estradiol)

时间窗: Day 1 for itraconazole cohort, Day 11 for rifampin cohort

AUC for 24 hours for segesterone acetate and ethinyl estradiol

Maximum concentration (Cmax) of rifampin and itraconzaole on Annovera (segesterone acetate and ethinyl estradiol)

时间窗: Day 1 for itraconazole cohort, Day 11 for rifampin cohort

Cmax for segesterone acetate and ethinyl estradiol

次要结局

  • Safety - Number of Participants with Adverse Events(Screening through 14 days following Annovera removal)
  • Safety - Vital signs - systolic and diastolic blood pressure(Through study completion, an average of 4 months)
  • Safety - Vital signs - pulse(Through study completion, an average of 4 months)
  • Tolerability -Discontinuation rates(Through study completion, an average of 4 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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Annovera™ Drug-Drug Interaction Study | 临床试验