Dose Finding Study of Contraceptive Vaginal Ring With Different Estradiol Levels in Combination With Nestorone

Completed · Phase 2

Conditions studied: Suppression of Ovulation

In brief

This clinical trial investigates a new vaginal delivery system made of silicone rubber, containing Nestorone®, a 19-nor progesterone derivative and a low dose of serum estradiol (E2). The investigators plan to evaluate one-month data on the serum estradiol (E2) levels of three different contraceptive vaginal rings that contain a fixed dose of NES and escalating doses (75 µg/day, 100 µg/day, or 200 µg/day) of estradiol as the basis for selecting a CVR for a larger contraceptive efficacy trial.

Key facts

Study ID

NCT02626208

Run by

Premier Research

People needed

65

Starts

2016-01-01

Expected to finish

2017-03-01

Last updated by the study team

2017-08-15

Who can join

Age: 18 and older, up to 39. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Good general overall health with no chronic medical conditions that result in periodic exacerbations that require significant medical care.
• Age 18-39 years, inclusive, at the enrollment visit.
• Have a regular menstrual cycle 21-35 days in duration when not using hormonal contraception
• Have an intact uterus and both ovaries.
• Able and willing to comply with the protocol and sign an informed consent.
• Consistent use of effective contraception during the preceding cycle (note: women who use oral, transdermal, vaginal, implantable or intrauterine hormonal contraceptives in the preceding cycle must have discontinued at least 7 days prior to start of treatment and not had unprotected intercourse since discontinuing the method).
• Not at high risk for pregnancy, defined as consistently using a non-hormonal method of contraception (including Copper IUDs); have a surgically sterile male partner with a vasectomy; be abstinent; or be in a same-sex relationship from the start of treatment through study exit (including recovery period).
• Have a negative pregnancy test at the admission visit.
• Have a diastolic blood pressure (BP) ≤85 mm Hg and systolic BP ≤135 mm Hg after 5 minutes rest in sitting position at the admission visit.
• Willing to abstain from use of non-water based vaginal lubricant during the study.

You may not qualify if…

• Participating in another clinical trial involving an investigational product within the last 30 days (prior to screening) or planning to participate in another clinical trial during this study.
• Not living in the catchment area of the study site.
• Known hypersensitivity to progestins or estrogen.
• Contraindications to combined estrogen-progestin contraceptive use including:
• Thrombophlebitis or thromboembolic disorders.
• Past personal history of deep vein thrombophlebitis or thromboembolic disorders.
• History of venous thrombosis or embolism in a first-degree relative <55 years of age suggesting familial defect in blood coagulation system.
• History of thrombosis or embolism OR any other personal or family history which in the opinion of the investigator suggests increased risk.
• History of stroke.
• Known or suspected carcinoma of the breast.
• Carcinoma of the endometrium or other known or suspected estrogen-dependent neoplasia.
• Undiagnosed abnormal genital bleeding.
• Cholestatic jaundice of pregnancy or jaundice with prior hormonal contraceptive use.
• Hepatic adenomas or carcinomas.
• Known or suspected pregnancy.
• Smoking in women who are 35 years and over or will be 35 years during the course of the trial; women <35 years who smoke 15 cigarettes or more per day must be evaluated by the investigator for inclusion based on risk factors that would increase their risk for cardiovascular disease (CVD) and thromboembolism, e.g. lipid levels, glucose level, BP, BMI, family history of CVD at a young age.
• History of retinal vascular lesions, unexplained partial or complete loss of vision.
• Headaches with focal neurological symptoms (e.g., migraines with auras).
• Desire to become pregnant during the study.
• Breastfeeding.
• Undiagnosed vaginal discharge or vaginal lesions or abnormalities. Subjects diagnosed at screening with a Chlamydia or gonococcus infection may be included in the trial following treatment; partner treatment is also recommended. Subjects with vaginal infection (yeast, trichomonis, or bacterial vaginosis) may be enrolled after treatment. Investigators should make a determination if subjects are at high risk for reinfection, e.g. multiple sex partners, untreated partner, and whether such subjects can be included. In accordance with PI/medical designee assessment and local standards of practice, women with a history of genital herpes can be included if outbreaks are infrequent.
• A known clinically significant Pap test abnormality, as managed by current local or national guidelines that will require treatment during study participation.
• Known benign or malignant liver tumors; known active liver disease.
• Invasive cancer (past history of any carcinoma or sarcoma, except non-melanoma skin cancer).
• Current or past medically diagnosed severe depression, which, in the opinion of the investigator, could be exacerbated by use of a hormonal contraceptive.

Where it is running

• University of California, Davis — Sacramento, California, United States
• Columbia University — New York, New York, United States
• University of Cincinnati — Cincinnati, Ohio, United States
• Oregon Health & Science Unit — Portland, Oregon, United States
• University of Pennsylvania — Philadelphia, Pennsylvania, United States
• University of Utah — Salt Lake City, Utah, United States
• Eastern Virginia Medical School (EVMS) — Norfolk, Virginia, United States

Full record on ClinicalTrials.gov

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