CONRAD, Department of Obstetrics and Gynecology, Eastern Virginia Medical School, Norfolk, VA.
Mapp Biopharmaceutical, Inc, San Diego, CA.
Am J Obstet Gynecol. 2023 Jun;228(6):716.e1-716.e12. doi: 10.1016/j.ajog.2023.02.024. Epub 2023 Mar 2.
With an unplanned pregnancy rate of 50% or more in many countries, there is an urgent need for contraceptives that are more accessible and acceptable. To meet the growing demand for new contraceptives, ZabBio developed ZB-06, a vaginal film containing HC4-N, a human contraceptive antibody that inactivates sperm.
This study aimed to assess the potential contraceptive activity of the ZB-06 film using a surrogate assessment for contraceptive efficacy, the postcoital test. We also assessed clinical safety of film use among healthy heterosexual couples. Serum, cervical mucus, and vaginal fluid HC4-N antibody concentrations and sperm agglutination potency were determined after single film use. Changes in the concentration of soluble proinflammatory cytokines and vaginal Nugent score after film use were measured as subclinical safety endpoints.
This was a phase 1, first-in-woman, open-label, proof-of-concept, postcoital test and safety study.
A total of 20 healthy women were enrolled in the study, and 8 heterosexual couples completed all study visits. The product was safe for both female participants and their male sexual partners. The postcoital test performed on ovulatory cervical mucus at baseline (no product use) revealed a mean of 25.9 (±30.6) progressively motile sperm per high-power field. After use of a single ZB-06 film before intercourse, this number dropped to 0.04 (±0.06) progressively motile sperm per high-power field (P<.0001). At the follow-up postcoital test visit approximately 1 month later (no product use), a mean of 47.4 (±37.4) progressively motile sperm per high-power field was observed, indicating contraceptive reversibility.
A single dose of the ZB-06 film applied before intercourse was safe and met efficacy surrogate benchmarks of excluding progressively motile sperm from ovulatory cervical mucus. These data indicate that ZB-06 is a viable contraceptive candidate warranting further development and testing.
在许多国家,未计划妊娠率高达 50%或更高,因此迫切需要更易获得和接受的避孕方法。为满足对新型避孕方法不断增长的需求,ZabBio 公司研发了 ZB-06 阴道薄膜,其含有可使精子失活的人用避孕抗体 HC4-N。
本研究旨在通过评估对避孕效果的替代指标即性交后试验,来评估 ZB-06 薄膜的潜在避孕活性。我们还评估了健康异性恋夫妇使用薄膜的临床安全性。在单次使用薄膜后,检测血清、宫颈黏液和阴道液中的 HC4-N 抗体浓度和精子凝集能力。使用薄膜后,作为亚临床安全性终点,还测量了可溶性促炎细胞因子浓度和阴道 Nugent 评分的变化。
这是一项在女性中首次进行的、开放标签的、概念验证性的、性交后试验和安全性研究。
本研究共纳入 20 名健康女性,其中 8 对异性恋夫妇完成了所有研究访视。该产品对女性参与者及其男性性伴侣均安全。在基线(无产品使用)时对有排卵的宫颈黏液进行的性交后试验显示,每个高倍视野中平均有 25.9(±30.6)条渐进性运动精子。在性交前使用单次 ZB-06 薄膜后,这一数字下降至 0.04(±0.06)个渐进性运动精子/高倍视野(P<.0001)。在大约 1 个月后的后续性交后试验访视(无产品使用)时,观察到每个高倍视野中有 47.4(±37.4)条渐进性运动精子,表明避孕具有可逆性。
单次剂量的 ZB-06 薄膜在性交前使用是安全的,并符合排除有排卵宫颈黏液中渐进性运动精子的替代疗效指标。这些数据表明,ZB-06 是一种有前途的避孕候选方法,值得进一步开发和测试。