Contraceptive Development Program; Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD.
Clin Chem. 2019 Jan;65(1):153-160. doi: 10.1373/clinchem.2018.295089.
Development of new methods of male contraception would address an unmet need for men to control their fertility and could increase contraceptive options for women. Pharmaceutical research and development for male contraception was active in the 1990s but has been virtually abandoned. The Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) has supported a contraceptive development program since 1969 and supports the majority of hormonal male contraceptive development. Nonhormonal methods are also in development but are at earlier stages.
Several hormonal male contraceptive agents have entered clinical trials. Single-agent products being evaluated include dimethandrolone undecanoate, 11β-methyl-nortestosterone dodecyl carbonate, and 7α-methyl-19-nortestosterone. A contraceptive efficacy trial of Nestorone gel and testosterone gel in a single application will begin in 2018. Potential nonhormonal methods are at preclinical stages of development. Many nonhormonal male contraceptive targets that affect either sperm production or sperm function have been identified. Targeted pathways include the retinoic acid pathway, bromodomain and extraterminal proteins, and pathways for Sertoli cell-germ cell adhesion or sperm motility. Druggable targets include CatSper, the sperm Na+/K+-exchanger, TSSK, HIPK4, EPPIN, and ADAMs family proteins. Development of a procedure to reversibly block the vas deferens (initially developed in India in the 1980s) is undergoing early stage research in the US under the trade name Vasalgel™.
NICHD has supported the development of reversible male contraceptive agents. Other organizations such as the World Health Organization and the Population Council are pursuing male contraceptive development, but industry involvement remains dormant.
开发新的男性节育方法将满足男性控制生育能力的未满足需求,并可为女性提供更多的避孕选择。20 世纪 90 年代,男性节育的药物研发十分活跃,但后来几乎被放弃。自 1969 年以来,美国国立儿童健康与人类发展研究所(NICHD)一直支持避孕药物开发项目,并支持大多数激素男性节育药物的开发。非激素方法也在开发中,但处于早期阶段。
几种激素男性避孕药已进入临床试验。正在评估的单一制剂产品包括二甲双雄醇十一酸酯、11β-甲基-诺龙十二碳酸酯和 7α-甲基-19-诺龙。2018 年将开始进行 Nestorone 凝胶和睾酮凝胶单次应用的避孕功效试验。潜在的非激素方法处于临床前开发阶段。许多影响精子生成或精子功能的非激素男性节育靶点已被确定。靶向途径包括维甲酸途径、溴结构域和末端蛋白以及 Sertoli 细胞-生殖细胞黏附或精子运动的途径。有针对性的药物靶点包括 CatSper(精子 Na+/K+-交换器)、精子 Na+/K+-交换器、TSSK、HIPK4、EPPIN 和 ADAMs 家族蛋白。可逆性阻断输精管的方法(最初于 20 世纪 80 年代在印度开发)正在美国进行早期研究,其商品名为 Vasalgel™。
NICHD 支持可逆男性节育药物的开发。其他组织,如世界卫生组织和人口理事会,也在追求男性节育药物的开发,但行业参与仍然处于休眠状态。