Evaluation of Efficacy, Safety and Tolerability of VeraCept IUS

A Phase 3, Prospective, Multi-Center, Single-Arm, Open-Label Study to Evaluate VeraCept®, a Long-Acting Reversible Intrauterine Contraceptive for Contraceptive Efficacy, Safety, and Tolerability

To assess the contraceptive efficacy (prevention of pregnancy) of VeraCept

Study Overview

• Status: Active, not recruiting
• Conditions: Women at Risk for Pregnancy
• Intervention / Treatment: Drug: VeraCept

Detailed Description

Study Design:

Prospective, multi-center, single-arm, open-label, Phase 3 clinical study to 3 years with extension up to 8 years

Number of Subjects:

Approximately 1,605 subjects will be enrolled into the study

Study Population:

Post-menarcheal, pre-menopausal women up to age 45 years, who are at risk for pregnancy and who desire a long-term intrauterine contraceptive for birth control will be eligible for this study.

Primary Endpoint:

The primary endpoint is the contraceptive efficacy through 3 years of use, as assessed by the Pearl Index.

Secondary endpoints:

Contraceptive Efficacy:

• Pearl Index at Years 4, 5, 6, 7 and 8 as well as cumulatively through Years 4, 5, 6, 7 and 8.
• Pregnancy percentage by life table analysis (Kaplan-Meier) at Years 1, 2, 3, 4, 5, 6, 7 and 8
• The cumulative Pearl Index for Years 6 to 8 will be calculated as well as the cumulative pregnancy percentage for Years 6 to 8 using a life table analysis (Kaplan-Meier) only for the EP population.

Study drug placement:

• Ease of VeraCept placement
• Placement success

Safety:

• Serious adverse events (SAEs)
• Adverse events (AEs)
• Pelvic infection (pelvic inflammatory disease (PID) or endometritis)
• Ectopic pregnancies
• Uterine perforations
• Dysmenorrhea
• Abdominal pain
• Expulsion rates at Years 1, 2, 3, 4, 5, 6, 7 and 8

Tolerability:

• Bleeding and spotting patterns
• Insertion pain assessed immediately after insertion
• Continuation rates at Years 1, 2, 3, 4, 5, 6, 7 and 8
• Reasons for discontinuation

Return to fertility

● Pregnancy rate in subjects who request VeraCept removal specifically to become pregnant. Subjects who desire pregnancy after having VeraCept removed will be followed for either 1 year, until they decide to no longer try to conceive or they become pregnant, whichever comes first.

• Study Type: Interventional
• Enrollment (Actual): 1620
• Phase: Phase 3

Contacts and Locations

Study Locations

• United States
  • Arizona
    • Scottsdale, Arizona, United States, 85251
      • MomDoc Women's Health Research
    • Tucson, Arizona, United States, 85712
      • Copperstate OB/GYN Associates
  • California
    • Berkeley, California, United States, 94710
      • Essential Access Health
    • Los Angeles, California, United States, 90010
      • Essential Access Health
    • Pomona, California, United States, 91767
      • Empire Clinical Research
    • Sacramento, California, United States, 95817
      • University of California, Davis Health System
    • San Diego, California, United States, 92111
      • M3 Wake Research (formerly Women's Health Care Research)
    • San Diego, California, United States, 92120
      • M3 Wake Research (formerly Medical Center for Clinical Research)
    • Stanford, California, United States, 94305
      • Stanford University, Medical Center, Obstetrics and Gynecolocy
  • Colorado
    • Englewood, Colorado, United States, 80110
      • Velocity Clinical Research (formerly Downtown Women's Health Care)
  • Florida
    • Lake Worth, Florida, United States, 33461
      • Altus Research, Inc
  • Georgia
    • Atlanta, Georgia, United States, 30308
      • Emory University School of Medicine
    • Decatur, Georgia, United States, 30034
      • Soapstone Center for Clinical Research
  • Idaho
    • Idaho Falls, Idaho, United States, 83404
      • Clinical Research Prime
  • Indiana
    • Fort Wayne, Indiana, United States, 46825
      • Women's Health Advantage
    • Indianapolis, Indiana, United States, 46202
      • Indiana University
  • Louisiana
    • Marrero, Louisiana, United States, 70072
      • Praetorian Pharmaceutical Research
  • Michigan
    • Ann Arbor, Michigan, United States, 48109
      • University of Michigan Von Voigtlander Women's Hospital
  • Minnesota
    • Minneapolis, Minnesota, United States, 55408
      • Planned Parenthood North Central States - Minneapolis
  • Missouri
    • Manchester, Missouri, United States, 63088
      • Planned Parenthood Great Rivers (formerly Planned Parenthood of the St. Louis Region and Southwest Missouri)
  • Nevada
    • Las Vegas, Nevada, United States, 89128
      • Rex Garn Mabey Jr., MD
  • New Jersey
    • Lawrenceville, New Jersey, United States, 08648
      • Capital Health Lawrence OBGYN Research (formerly Lawrence OB/Gyn Clinical Research)
  • New York
    • New York, New York, United States, 10032
      • Columbia University Medical Center, Division of Family Planning
  • North Carolina
    • Durham, North Carolina, United States, 27710
      • Duke University Medical Center
  • Ohio
    • Cincinnati, Ohio, United States, 45267
      • University of Cincinnati/Reproductive Medicine Research
    • Columbus, Ohio, United States, 43210
      • The Ohio State University Ob/Gyn Research Office
  • Oregon
    • Portland, Oregon, United States, 97239
      • OHSU Women's Health Research Unit
  • Pennsylvania
    • Philadelphia, Pennsylvania, United States, 19114
      • Clinical Research of Philadelphia
    • Philadelphia, Pennsylvania, United States, 19104
      • University of Pennsylvania/Penn Family Planning and Pregnancy Loss Center
    • Pittsburgh, Pennsylvania, United States, 15213
      • Magee-Womens Hospital, Center for Family Planning Research
  • South Carolina
    • Charleston, South Carolina, United States, 29407
      • Medical Research South, LLC
  • Tennessee
    • Chattanooga, Tennessee, United States, 37404
      • Chattanooga Medical Research
    • Jackson, Tennessee, United States, 38305
      • The Jackson Clinic, PA
  • Texas
    • Corpus Christi, Texas, United States, 78414
      • Advanced Research Associates
    • Pearland, Texas, United States, 77584
      • Advances in Health
  • Utah
    • Salt Lake City, Utah, United States, 84132
      • University of Utah Healthcare Health Sciences Center
    • Salt Lake City, Utah, United States, 84107
      • Wasatch Clinical Research
  • Virginia
    • Norfolk, Virginia, United States, 23502
      • Tidewater Physicians for Women
    • Norfolk, Virginia, United States, 23507
      • Eastern Virginia Medical
  • Washington
    • Seattle, Washington, United States, 98117
      • University of Washington Medical Center
    • Seattle, Washington, United States, 98104
      • Seattle Clinical REsearch Center (formerly Seattle Women's Health)

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: No older than 45 years (Child, Adult)
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

1. Post-menarcheal, pre-menopausal females up to 45 years of age at the time of informed consent/assent and in good general health;
2. History of regular menstrual cycles defined as occurring every 21-35 days when not using hormones or prior to recent pregnancy or spontaneous or induced abortion;
3. Sexually active with a male partner who has not had a vasectomy;
4. Reasonably expect to have coitus at least once monthly during the study period;
5. In a mutually monogamous relationship of at least 3 months duration;
6. Seeking to avoid pregnancy for the duration of the study;
7. Willing to use the study drug as the sole form of contraception;
8. Willing to accept a risk of pregnancy;
9. Subjects must be in compliance with cervical cancer screening guidelines per the American Society for Colposcopy and Cervical Pathology (ASCCP) guidelines without evidence of disease. Subjects who are age 21-24 y/o, at time of informed consent, must have a normal Papanicolaou test (Pap), atypical squamous cells of undetermined significance (ASC-US), or low-grade squamous intraepithelial lesion (LSIL). Subjects who are 25 or older at the time of informed consent with ASC-US results, must also have a negative high-risk human papilloma virus (HPV) test result within the appropriate screen timeframe per American Society for Colposcopy and Cervical Pathology (ASCCP) guidelines, and prior to the study IUS insertion. Alternatively, the subject must have had a colposcopy performed within the appropriate screen timeframe, and prior to the study IUS insertion that showed no evidence of dysplasia requiring treatment per ASCCP guidelines, or treatment was performed and follow-up at least 6 months after the treatment showed no evidence of disease by clinical evaluation;
10. Able and willing to comply with all study tests, procedures, assessment tools (including e-diary) and follow-up;
11. Able and willing to provide and document informed consent and Authorization for Release of Protected Health Information (PHI). Unemancipated subjects under 18 years old must provide assent and have written parental consent documented on the consent form consistent with local legal requirements;
12. Plan to reside within a reasonable driving distance of a research site for the duration of the study.
13. Subject agrees not to self-remove VeraCept

Exclusion Criteria:

1. Known or suspected pregnancy; or at risk for pregnancy from unprotected intercourse earlier in current cycle;
2. Subject who anticipates separation from her partner for more than a 6-month period during use of VeraCept;
3. A previously inserted intrauterine system (IUS) that has not been removed by the time the study IUS is placed;
4. History of previous IUS complications, such as perforation, expulsion, or pregnancy with IUS in place;
5. Pain with current IUS;
6. Injection of hormonal contraceptive (e.g., Depo-Provera) within the last 10 months and has not had 2 normal menstrual cycles since the last injection;
7. Planned use of any non-contraceptive estrogen, progesterone or testosterone any time during study participation;
8. Exclusively breastfeeding before return of menses; lactating women will be excluded unless they have had 2 normal menstrual periods prior to enrollment;
9. Unexplained abnormal uterine bleeding (suspicious for a serious condition), including bleeding 4 weeks post-septic abortion or puerperal sepsis;
10. Severely heavy or painful menstrual bleeding;
11. Suspected or known cervical, uterine or ovarian cancer, or unresolved clinically significant abnormal Pap smear requiring evaluation or treatment;
12. Any history of gestational trophoblastic disease with or without detectable elevated ß-human chorionic gonadotropin (ß-hCG) levels, or related malignant disease;

13. Any congenital or acquired uterine anomaly that may complicate study drug placement, such as:

    • Submucosal uterine leiomyoma
    • Asherman's syndromes
    • Pedunculated polyps
    • Bicornuate uterus
    • Didelphus or uterine septa
14. Any distortions of the uterine cavity (e.g. fibroids), that, in the opinion of the investigator, are likely to cause issues during insertion, retention or removal of the IUS;
15. Known anatomical abnormalities of the cervix such as severe cervical stenosis, prior trachelectomy or extensive conization that, in the opinion of the investigator would prevent cervical dilation and study drug placement;
16. Untreated or unresolved acute cervicitis or vaginitis;
17. Known or suspected human immunodeficiency virus (HIV) infection or clinical AIDS;
18. Subjects who have an established immunodeficiency;
19. Known intolerance or allergy to any components of VeraCept including intolerance or allergy to nickel, titanium, or copper, and including Wilson's Disease;
20. Currently participating or planning future participation in a research study of an investigational drug or device during the course of this investigational study. Subject must have waited at least 30 days from exiting their last study prior to informed consent in this study;
21. Subject has been enrolled in a previous VeraCept or LevoCept study; 21a. Subject has been enrolled in a previous VeraCept or LevoCept study where VeraCept or LevoCept placement was successful or attempted (replaces exclusion #21 for PK sub-study subjects only);
22. Known or suspected alcohol or drug abuse within 12 months prior to the screening visit;
23. Any general health, mental health or behavioral condition that, in the opinion of the investigator, could represent an increased risk for the subject or would render the subject less likely to provide the needed study information;
24. Study staff or a member of the immediate family of study staff.
25. Subject is <4 weeks post-pregnancy (postpartum, spontaneous or induced abortion)

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: VeraCept; VeraCept® Intrauterine Contraceptive	Drug: VeraCept; VeraCept Intrauterine Contraceptive is a hormone free, low dose, copper-releasing birth control method

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Contraceptive Efficacy Through 3 Years of Use	Contraceptive efficacy through 3 years of use, as assessed by the Pearl Index. The Pearl Index is calculated as the number of on-treatment pregnancies per 100 woman-years of exposure. On-treatment pregnancy is defined as the estimated conception date being on or after the insertion date (must be a successful insertion) and no more than 7 days after the study drug is removed or expelled. One women year is defined as comprising thirteen 28-day cycles. A lower Pearl Index indicates greater contraceptive effectiveness.	3 years

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Contraceptive Efficacy at Years 4, 5, 6, 7 and 8	Pearl Index will be calculated for Years 4, 5, 6, 7, and 8 as well as cumulatively through Years 4, 5, 6, 7, and 8	Years 4, 5, 6, 7, and 8 and cumulatively through Years 4, 5, 6, 7, and 8
Cumulative Pregnancy Percentage	A life table analysis (using Kaplan-Meier) of pregnancies will be performed for the EP population to present the cumulative pregnancy percentage	Years 1 through 3
Ease of VeraCept Placement	Ease of VeraCept placement will be summarized for the ITT population as reported by the investigator (Very easy, Easy, Neither Easy nor Hard, Hard, Very Hard). (First Attempt)	Visit 1 (Day 1) / VeraCept placement
VeraCept Placement Success	The number and percentage of subjects with either a successful or unsuccessful placement will be summarized for the ITT	Visit 1 (Day 1) / VeraCept placement
Bleeding and Spotting Patterns	Bleeding and spotting patterns will be summarized for the first year of treatment by the number of days in each 28-day cycle with bleeding or spotting, bleeding only, and spotting only	Through year 1
Insertion Pain Assessed Immediately After Insertion (First Attempt)	Insertion pain summarized for subjects at first attempt as reported by the subjects	Visit 1 (Day 1), immediately after insertion
Cumulative VeraCept Discontinuation Rates	Cumulative VeraCept discontinuation rates will be summarized using Kaplan-Meier methods for the Safety population.	Years 1 through 3
Cumulative VeraCept Expulsion Rates	Cumulative VeraCept expulsion rates will be summarized using Kaplan-Meier methods for the Safety population.	Years 1 through 3
Return to Fertility. Only for Subjects Requesting VeraCept Removal to Become Pregnant.	The number and percentage of subjects with each return to fertility response will be summarized for the Safety population.	Subjects will be followed for either 1 year, until they decide to no longer try to conceive or they become pregnant, whichever comes first.
Safety Adverse Events of Special Interest: Pelvic Infection (PID or Endometriosis), Uterine Perforations, and Abdominal Pain		3 years

Collaborators and Investigators

• Sponsor: Sebela Women's Health Inc.
• Collaborators: Syneos Health
• Investigators: Principal Investigator: David Turok, MD, MPH, University of Utah

Study record dates

Study Major Dates

• Study Start (Actual): August 22, 2018
• Primary Completion (Actual): September 22, 2022
• Study Completion (Estimated): September 22, 2027

Study Registration Dates

• First Submitted: July 19, 2018
• First Submitted That Met QC Criteria: August 14, 2018
• First Posted (Actual): August 16, 2018

Study Record Updates

• Last Update Posted (Actual): August 22, 2025
• Last Update Submitted That Met QC Criteria: August 5, 2025
• Last Verified: August 1, 2025

More Information

Terms related to this study

• Other Study ID Numbers: CMDOC-0042

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No