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首页> 外文期刊>AIDS Research and Human Retroviruses >A randomized male tolerance study of dapivirine gel following multiple topical penile exposures (MTN 012/IPM 010)
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A randomized male tolerance study of dapivirine gel following multiple topical penile exposures (MTN 012/IPM 010)

机译:多次局部阴茎暴露后达匹韦林凝胶的男性随机耐受研究(MTN 012 / IPM 010)

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摘要

Dapivirine (DPV) is a nonnucleoside reverse transcriptase inhibitor with a favorable safety profile following vaginal application. A penile tolerance study was conducted prior to further development of DPV as a candidate vaginal microbicide. Twenty-four circumcised and 24 uncircumcised (N=48) healthy HIV-negative male participants aged 18 years or older were randomized 2:1:1 to apply DPV 0.05% gel, matched placebo gel, or universal placebo gel, respectively, to their penis once daily for 7 sequential days. The safety, acceptability, and pharmacokinetic profile of DPV 0.05% gel were assessed by the presence of Grade 2 or higher genitourinary adverse events (AEs) and systemic AEs, a behavioral questionnaire, and pharmacokinetic plasma blood draw, respectively, at the final clinic visit (FCV). There were no Grade 2 genitourinary AEs in 47 participants completing the FCV. One participant in the DPV arm failed to attend the FCV. There were 13 AEs reported; all were Grade 1 except one Grade 2 corneal laceration unrelated to study product. Participants liked the gel to a moderate extent, yet 72% reported they would be "very likely" to use a gel like the one they used in the study every time they have intercourse. DPV was detectable in plasma in all 23 DPV arm study participants at the FCV. On average, the circumcised participants' DPV concentrations were 54% of those in uncircumcised participants (p=0.07). Topical seven-day penile application of DPV 0.05% gel was locally and systemically safe, was acceptable to male participants, and resulted in systemic exposure to the drug.
机译:Dapivirine(DPV)是一种非核苷类逆转录酶抑制剂,在阴道应用后具有良好的安全性。在进一步开发DPV作为阴道杀菌剂候选物之前,先进行了对阴茎的耐受性研究。将24岁,18岁或18岁以上未割包皮的健康的HIV阴性男性参与者和24名未割包皮的健康的HIV阴性男性参与者按2:1:1的比例随机分配DPV 0.05%凝胶,匹配的安慰剂凝胶或通用安慰剂凝胶阴茎连续7天每天一次。在最终临床访视时,分别通过是否存在2级或更高级别的泌尿生殖系统不良事件(AE)和全身性AE,行为调查表和药代动力学血浆抽血评估DPV 0.05%凝胶的安全性,可接受性和药代动力学特征(FCV)。完成FCV的47名参与者中没有2级泌尿生殖道AE。 DPV部门的一名参与者未能参加FCV。报告了13种AE。除与研究产品无关的2级角膜撕裂外,其余均为1级。参与者在某种程度上喜欢这种凝胶,但是72%的人报告说,他们“极有可能”每次性交时都使用他们在研究中使用的那种凝胶。在FCV的所有23位DPV臂研究参与者中,血浆中均可检测到DPV。平均而言,割包皮的参与者的DPV浓度是未割包皮的参与者的54%(p = 0.07)。 DPV 0.05%凝胶局部阴茎注射7天局部和全身安全,男性参与者可以接受,并导致全身性接触该药物。

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