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临床试验/NCT06263582
NCT06263582已完成1 期

Pharmacokinetics of Intravaginal, Self-administered Artesunate Vaginal Pessaries Among Women in Kenya

UNC Lineberger Comprehensive Cancer Center1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2024年5月29日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
16
试验地点
1
主要终点
To Determine the Area Under the Plasma Concentration Versus Time Curve (AUC) of Dihydroartemisinin

研究概览

简要总结

This study investigates the pharmacokinetics of Artesunate (AS) and dihydroartemisinin (DHA), the active metabolite of Artesunate, following intravaginal use at the dosing and frequency being studied for cervical precancer treatment. A secondary objective is to investigate safety among study participants.

详细描述

Due to lack of access to primary and secondary prevention, women living in low-and middle-income countries bear a disproportionate burden of cervical cancer, accounting for 90% of new cases and 85% of deaths globally. Cervical cancer can be prevented through vaccination against Human papillomavirus (HPV), whose infection is required to develop cervical cancer. Among unvaccinated women, screening for HPV or cervical precancer allows identification of precancerous lesions - primarily cervical intraepithelial neoplasia grade 2 or 3 (CIN2/3), that can be treated and cured, to prevent progression to cancer. Most CIN2/3 lesions that are left untreated will progress to invasive cervical cancer. Current treatments for CIN2/3 in both high- and low-resource countries (LMICs) require trained health care providers, who are often out of reach for many women, particularly in rural areas in LMICs. Lack of access to precancer treatment following screening in LMICs in part accounts for the high burden of incident cervical cancer. Preclinical data have demonstrated pro-apoptotic effects of Artesunate (AS), a commonly available drug with an excellent safety profile in oral, rectal and intravenous routes primarily used to treat malaria in LMICs. This led to a recent Phase I study in the United States that demonstrated that self-administered vaginal artesunate inserts (pessaries) are safe, well-tolerated, and demonstrate efficacy for treatment of CIN2/3. Based on the mechanism of action, the clinical safety profile, and widespread availability as a generic drug on the World Health Organization (WHO) List of Essential Medications, vaginal artesunate inserts (pessaries), if backed by data from randomized trials, may offer patient-controlled and access cervical precancer treatment method for women in LMICs who face the greatest burden of cervical cancer and have difficulty accessing skilled providers for precancer treatment. However, given that artesunate is a well-known drug used in malaria treatment, it is critical to ensure that vaginal application of the drug will not promote resistance for use in malaria treatment.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older 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

Artesunate vaginal inserts/ pessaries

Experimental

Artesunate vaginal inserts/pessaries are used as a treatment for cervical precancerous lesions.

干预措施: Artesunate pessary (Drug)

Artesunate vaginal inserts/ pessaries

Experimental

Artesunate vaginal inserts/pessaries are used as a treatment for cervical precancerous lesions.

干预措施: blood draws for pharmacokinetics of the study drug (Diagnostic Test)

结局指标

主要结局

To Determine the Area Under the Plasma Concentration Versus Time Curve (AUC) of Dihydroartemisinin

时间窗: Day 5

To determine the area under the plasma concentration versus time curve (AUC) of dihydroartemisinin (DHA) following five consecutive days of self-administration of 200mg Artesunate vaginal inserts (pessaries). Mean DHA AUC will be submitted.

次要结局

  • To Determine the Time to Maximum Concentration (Tmax) of Artesunate (AS) Following Five Consecutive Days(Day 5)
  • To Determine the Time to Maximum Concentration (Tmax) of Dihydroartemisinin (DHA(Day 5)
  • To Determine the Half-life (t1/2) of Dihydroartemisinin (DHA)(Day 5)
  • To Determine the Apparent Clearance (CL/F) of Dihydroartemisinin (DHA)(Day 5)
  • To Determine the Volume of Distribution (V/F) of Artesunate (AS)(Day 5)
  • To Determine the Volume of Distribution (V/F) of Dihydroartemisinin (DHA)(Day 5)
  • Type, Frequency, Severity, and Duration of Adverse Events(Up to day 10 days)
  • To Determine the Maximum Concentration of Artesunate (AS)(Day 5)
  • To Determine the Maximum Concentration of Dihydroartemisinin (DHA) (Cmax)(Day 5)
  • To Determine the Area Under the Plasma Concentration Versus Time Curve (AUC) of Artesunate (AS)(Day 5)
  • To Determine the Half-life (t1/2) of Artesunate (AS)(Day 5)
  • To Determine the Apparent Clearance (CL/F) of Artesunate (AS)(Day 5)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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