The contraceptive ring (CR) is a method for delivering steroids by vaginal route for fertility control. The project describes our plans to study a CR containing a combination of norethindrone acetate (NET Ac: 13beta-methyl- 17alpha-ethynyl-17beta-acetoxy-19-norandrosten-4-en-3-one) and ethynylestradiol (EE: 17alpha-ethynyl-1,3,5,(10)-estratriene-3,17beta- diol). This device could be an important addition to modern forms of contraception. It provides a special advantage to women who wish to have the initiation and termination of a contraceptive method under their own control. In previous studies, a wide range of dose combinations were tested in a CR that provided protection from pregnancy for three months. To date, rings that deliver a dose of NET Ac/EE of 1 mg/20 mug inhibit ovulation and control bleeding well. These Phase 2 studies will be completed to establish the lowest dose of EE necessary in combination with 1 mg of NET Ac to effectively control bleeding patterns, inhibit ovulation, and produce minimal effects on lipid patterns. The CRs for these studies will be made in the laboratories of the Population Council. The Population Council has established a relationship with a commercial partner, and will transfer technology for manufacture of CRs that deliver the agreed doses. The commercially-manufactured CRs will be tested both in vivo and in a Phase 2 study to confirm that they perform as well as the Population Council's handmade CRs. A study will be conducted on the final NET Ac/EE dosage selected to investigate variations in the CR insertion schedule on the first day of each cycle to minimize side effects. This same study will also give information on the acceptability of CRs. Stability studies will be performed on the manufactured CRs to establish the product's shelf life. Finally, a Phase 3 study will be conducted on the manufactured CRs to determine acceptability, effectiveness, control of menstrual bleeding, and any possible side effects. The goal is to apply for a New Drug Application and register the CR in the United States.

Project Start
2000-03-01
Project End
2001-02-28
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
9
Fiscal Year
2000
Total Cost
$230,637
Indirect Cost
Name
Population Council
Department
Type
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10017
Xiao, Xiang; Ni, Ya; Yu, Chenhuan et al. (2018) Src family kinases (SFKs) and cell polarity in the testis. Semin Cell Dev Biol 81:46-53
Chen, Haiqi; Mruk, Dolores D; Lui, Wing-Yee et al. (2018) Cell polarity and planar cell polarity (PCP) in spermatogenesis. Semin Cell Dev Biol 81:71-77
Chen, Haiqi; Xiao, Xiang; Lui, Wing-Yee et al. (2018) Vangl2 regulates spermatid planar cell polarity through microtubule (MT)-based cytoskeleton in the rat testis. Cell Death Dis 9:340
Wen, Qing; Mruk, Dolores; Tang, Elizabeth I et al. (2018) Cell polarity and cytoskeletons-Lesson from the testis. Semin Cell Dev Biol 81:21-32
Li, Linxi; Mao, Baiping; Wu, Siwen et al. (2018) Regulation of spermatid polarity by the actin- and microtubule (MT)-based cytoskeletons. Semin Cell Dev Biol 81:88-96
Wen, Qing; Tang, Elizabeth I; Li, Nan et al. (2018) Regulation of Blood-Testis Barrier (BTB) Dynamics, Role of Actin-, and Microtubule-Based Cytoskeletons. Methods Mol Biol 1748:229-243
Chen, Shuhua; Kumar, Narender; Mao, Zisu et al. (2018) Therapeutic progestin segesterone acetate promotes neurogenesis: implications for sustaining regeneration in female brain. Menopause 25:1138-1151
Chen, Haiqi; Lui, Wing-Yee; Mruk, Dolores D et al. (2018) Monitoring the Integrity of the Blood-Testis Barrier (BTB): An In Vivo Assay. Methods Mol Biol 1748:245-252
Wen, Qing; Tang, Elizabeth I; Gao, Ying et al. (2018) Signaling pathways regulating blood-tissue barriers - Lesson from the testis. Biochim Biophys Acta Biomembr 1860:141-153
Mao, Baiping; Mruk, Dolores; Lian, Qingquan et al. (2018) Mechanistic Insights into PFOS-Mediated Sertoli Cell Injury. Trends Mol Med 24:781-793

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