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临床试验/NCT02166502
NCT02166502已完成不适用

Nevirapine Dosing in Neonates for Prophylaxis of Mother-to-Child-Transmission (MTCT) of HIV Infection

The Hospital for Sick Children2 个研究点 分布在 1 个国家目标入组 27 人开始时间: 2012年2月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
27
试验地点
2
主要终点
Proportion of nevirapine trough (Cmin) plasma levels that are above or below the target range for prophylaxis

研究概览

简要总结

The purpose of this study is to determine whether the current dose of nevirapine recommended in the Ontario Ministry of Health vertical transmission prevention protocol achieves therapeutic drug levels in newborn infants at high risk of HIV infection.

详细描述

Although nevirapine (NVP) is often given as part of combination antiretroviral therapy (cART) at our institutions for prevention of vertical transmission (VT) in high risk infants, the optimal prophylactic dose of nevirapine is unknown. The National Institute of Health (NIH) guidelines currently recommend a single 2 mg/kg dose of nevirapine given to the infant within 72 hours of birth, however, this dose is not being used in practice given the controversies previously described with single-dose nevirapine. In the absence of any guidance to inform the multiple daily dosing of nevirapine for prophylaxis of VT, we are currently using the treatment dose for infants >15 days of age of 150 mg/m2 once daily for 14 days, then increasing to 150 mg/m2 twice daily for 14 days. This is analogous to the treatment dosing of triple antiretrovirals (ARVs) that is given for occupational post-exposure prophylaxis. Nevirapine is given for 4 weeks total with zidovudine (AZT) and lamivudine (3TC), followed by 2 additional weeks of AZT and 3TC to prevent the development of nevirapine resistance from its long half life. Stopping all 3 drugs simultaneously would result in a period of functional NVP monotherapy, resulting in a risk of NVP resistance should the infant become infected despite prophylaxis. Since the dose of nevirapine being used in our clinic populations for prevention of VT is higher than has been previously studied in neonates, it is important to evaluate the safety and efficacy of this dosing regimen, using therapeutic drug monitoring.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
— 至 72 Hours(Child)
性别
All
接受健康志愿者

入选标准

  • Newborn infants prescribed combination antiretroviral treatment with nevirapine for prevention of mother-to-child HIV transmission. These infants are routinely referred to the Hospital for Sick Children (SickKids) and Children's Hospital of Eastern Ontario (CHEO) HIV clinics in Toronto and Ottawa, respectively, for ongoing management. The majority of referrals are from Mount Sinai Hospital and St. Michael's Hospital in Toronto, and the Ottawa General Hospital in Ottawa.
  • Voluntary informed consent by the legal guardian

排除标准

  • Infants born prior to 32 weeks gestational age;
  • Infants with life-threatening medical conditions;
  • Infants unable to take oral medication;
  • Infants born to women considered at high risk of harboring nevirapine resistance mutations in whom Kaletra (lopinavir/ritonavir) is a therapeutic option (e.g. term neonates) will be excluded and prescribed Kaletra rather than nevirapine

结局指标

主要结局

Proportion of nevirapine trough (Cmin) plasma levels that are above or below the target range for prophylaxis

时间窗: Weeks 1, 2, and 4

次要结局

  • Final dose of nevirapine(Week 4)
  • Derived pharmacokinetic parameters(Week 4)
  • Association between nevirapine levels and incidence of adverse effects(Weeks 1, 2 and 4)
  • Association between patient characteristics and differences in nevirapine levels(Baseline, Week 1, 2 and 4)
  • Rate of vertical transmission of HIV(18 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ari Bitnun

Staff Physician

The Hospital for Sick Children

研究点 (2)

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