这是一项为期1年的前瞻性、开放标签、单臂、多中心、3期临床试验,目的是研究口服孕激素单药4mg drospirenone的避孕效果和安全性,采用24/4天的治疗方案

Q2 Medicine
Thomas Kimble , Anne E. Burke , Kurt T. Barnhart , David F. Archer , Enrico Colli , Carolyn L. Westhoff
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引用次数: 26

摘要

目的评价美国口服螺螺酮4 mg / 24 - 4天方案的避孕效果和安全性。研究设计:我们在性活跃的女性中进行了一项前瞻性、单臂、多中心的3期试验,为期13个28天的治疗周期。主要终点是Pearl指数,使用年龄≤35 岁的非母乳喂养妇女中确认的非药物妊娠和可评估周期来计算。我们评估了不良事件(ae),包括高钾血症和静脉血栓栓塞。结果1006名接受至少一剂屈螺酮治疗的女性中,352名(35.0%)完成了试验,654名(65.0%)在试验结束前停止了治疗。大多数参与者(92.2%)年龄 ≤35 岁;1 / 3体重指数(BMI)≥30 kg/m2。年龄≤35 岁的非母乳喂养妇女中,有17例妊娠(Pearl指数:4.0;95%置信区间[CI], 2.3-6.4;n = 953),其中3个未经证实,2个来自因严重违反食品药品监督管理局规定而被排除在主要分析之外的站点。在915名年龄≤35 岁的非母乳喂养妇女中确认怀孕的Pearl指数为2.9 (95% CI: 1.5-5.1)。几乎所有(95.4%)治疗后出现的ae都是轻度或中度的。无静脉血栓栓塞病例报告。高钾血症发生率为0.5%。基线收缩压/舒张压 ≥ 130/85 mmHg的女性在出院时血压平均较基线降低(- 8.5/ - 4.9 mmHg;n = 119)。未观察到其他临床相关的变化。参与者的满意度很高。结论吡螺酮4 mg 24/4方案在包括超重或肥胖妇女在内的广泛妇女群体中具有良好的安全性/耐受性,是一种有效的避孕方案。这种新的纯孕激素避孕药,螺螺酮4 mg, 24/4疗程,为大多数女性提供了一种避孕选择,无论血压或体重指数如何。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A 1-year prospective, open-label, single-arm, multicenter, phase 3 trial of the contraceptive efficacy and safety of the oral progestin-only pill drospirenone 4 mg using a 24/4-day regimen

A 1-year prospective, open-label, single-arm, multicenter, phase 3 trial of the contraceptive efficacy and safety of the oral progestin-only pill drospirenone 4 mg using a 24/4-day regimen

A 1-year prospective, open-label, single-arm, multicenter, phase 3 trial of the contraceptive efficacy and safety of the oral progestin-only pill drospirenone 4 mg using a 24/4-day regimen

Objectives

To evaluate contraceptive effectiveness and safety of oral drospirenone 4 mg 24/4-day regimen in the United States.

Study design

We performed a prospective, single-arm, multicenter phase 3 trial in sexually active women for up to thirteen 28-day treatment cycles. Primary outcome was the Pearl index, calculated using confirmed on-drug pregnancies and evaluable cycles in nonbreastfeeding women aged ≤ 35 years. We assessed adverse events (AEs), including hyperkalemia and venous thromboembolism.

Results

Of 1006 women who received at least one dose of drospirenone, 352 women (35.0%) completed the trial and 654 (65.0%) women discontinued before trial end. Most participants (92.2%) were ≤ 35 years; one third had a body mass index (BMI) ≥ 30 kg/m2. Among nonbreastfeeding women aged ≤ 35 years, there were 17 pregnancies (Pearl index: 4.0; 95% confidence interval [CI], 2.3–6.4; n = 953), of which three were unconfirmed and two were from sites excluded from the main analysis for major breaches of Food and Drug Administration regulations. The Pearl index was 2.9 (95% CI: 1.5–5.1) for confirmed pregnancies among 915 nonbreastfeeding women aged ≤ 35 years from sites with no protocol violations. Nearly all (95.4%) treatment-emergent AEs were mild or moderate in intensity. No cases of venous thromboembolism were reported. The frequency of hyperkalemia was 0.5%. Women with baseline systolic/diastolic blood pressure ≥ 130/85 mmHg had a mean reduction from baseline in blood pressure at exit visit (− 8.5/− 4.9 mmHg; n = 119). No other clinically relevant changes were observed. Participant satisfaction was high.

Conclusion

Drospirenone 4 mg 24/4 regimen provides effective contraception with a good safety/tolerability profile in a broad group of women, including overweight or obese women.

Implications

This new progestin-only contraceptive, drospirenone 4 mg in a 24/4 regimen, provides a contraceptive option for the majority of women regardless of blood pressure or BMI.

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来源期刊
Contraception: X
Contraception: X Medicine-Obstetrics and Gynecology
CiteScore
5.10
自引率
0.00%
发文量
17
审稿时长
22 weeks
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