TY - JOUR
T1 - Efficacy of the 1-year (13-cycle) segesterone acetate and ethinylestradiol contraceptive vaginal system
T2 - results of two multicentre, open-label, single-arm, phase 3 trials
AU - Archer, David F.
AU - Merkatz, Ruth B.
AU - Bahamondes, Luis
AU - Westhoff, Carolyn L.
AU - Darney, Philip
AU - Apter, Dan
AU - Jensen, Jeffrey T.
AU - Brache, Vivian
AU - Nelson, Anita L.
AU - Banks, Erika
AU - Bártfai, György
AU - Portman, David J.
AU - Plagianos, Marlena
AU - Dart, Clint
AU - Kumar, Narender
AU - Creasy, George W.
AU - Sitruk-Ware, Regine
AU - Blithe, Diana L.
N1 - Funding Information:
DFA within the past 3 years has received research support from Actavis, Bayer Healthcare, Endoceutics, Glenmark, Merck, Radius Health, Shionogi, and TherapeuticsMD; and has served as a consultant to AbbVie, Actavis, Agile Therapeutics, Bayer Healthcare, Endoceutics, Exeltis, InnovaGyn, Merck, Pfizer, Radius Health, Sermonix, Shionogi, Teva Women's Healthcare, and TherapeuticsMD. RBM is an employee of Population Council. CLW consults for or is on the advisory board of Allergan, Bayer Healthcare, Cooper Surgical, and Merck; and has received research support from Agile Therapeutics, Estetra SPRL, Leon Farma, and Medicines360. DA has received grant support from WHO for the conduct of this study. JTJ is on the advisory board of AbbVie, Bayer Healthcare, Merck, Population Council, and Sebela; and has received research support from AbbVie, Bayer Healthcare, Dare Bioscience, Estetra SRPL, Medicines360, Merck, National Institutes of Health (NIH), and National Institute of Child Health and Human Development (NICHD). ALN consults for or is on the advisory board of Agile Therapeutics, AMAG Technology, Bayer Healthcare, ContraMed/Sebela, Cooper Surgical, Merck, and Pharmanest; has received research support from Estetra, EvoFem, FHI (MonaLisa), and Mathra; and has served on the speaker's bureau of Agile Therapeutics, Avion, Bayer Healthcare, Cooper Surgical, and Merck. DJP consults for Agile Therapeutics and AMAG Technology; has received research support from Population Council; has served on the speaker's bureau of AMAG Technology and TherapeuticsMD; and is currently Chief Executive Officer of Sermonix with stock or stock options. MP is an employee of Population Council. CD is an employee of Health Decisions, which received research support from NICHD. NK is an employee of Population Council. GWC is an employee of Population Council. RS-W is an employee of Population Council. DLB is the Program Chief of the Contraceptive Development Program at the NICHD and directs the Contraceptive Clinical Trial Network. In that capacity, she was involved in a leadership role in the design of the study, conduct of the study, data analysis, interpretation of data, writing of the manuscript, and the decision to submit the paper for publication. All other authors declare no competing interests.
Funding Information:
We thank The Eunice Kennedy Shriver National Institute of Child Health and Human Development of the National Institutes of Health (NICHD), the US Agency for International Development (USAID), and WHO for funding the phase 3 studies. We also acknowledge all participating study investigators ( appendix p 1 ) and coordinators at the 27 clinical sites for conduct of the two phase 3 clinical trials and the over 2200 women participants from eight countries. We further acknowledge the medical writing assistance of Kathleen Ohleth (Precise Publications; Bedminster. NJ, USA) supported by TherapeuticsMD (Boca Raton, FL, USA). The NICHD (contract no HHSN27500403372 ) funded and conducted the US study and USAID (grant no GPO-A-00-04-00019-00 ) funded the international study, which was conducted by the Population Council. WHO Department of Reproductive Health and Research funded two international study sites. Medical writing support for manuscript submission and resubmission was supported by TherapeuticsMD. The authors acknowledge the major contribution of Daniel R Mishell Jr (deceased), from the Department of Obstetrics and Gynecology, University of Southern California, Keck School of Medicine (Los Angeles, CA, USA) who invented the concept of the vaginal system to deliver contraceptive steroids, did many of the clinical studies for the segesterone acetate and ethinylestradiol contraceptive vaginal system, and was a principle investigator for the 300 B phase 3 study analysed in this Article while a member of the International Committee for Contraceptive Research (ICCR) of the Population Council. The authors also gratefully acknowledge the contribution of Horacio B Croxatto, from the University of Chile (Santiago, Chile), who established the clinical centre in Chile, participated in all pivotal clinical studies for this ring, and provided guidance for the full development of this new contraceptive while a member of the ICCR.
Publisher Copyright:
© 2019 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY-NC-ND 4.0 license
PY - 2019/8
Y1 - 2019/8
N2 - Background: A ring-shaped, contraceptive vaginal system designed to last 1 year (13 cycles) delivers an average of 0·15 mg segesterone acetate and 0·013 mg ethinylestradiol per day. We evaluated the efficacy of this contraceptive vaginal system and return to menses or pregnancy after use. Methods: In two identically designed, multicentre, open-label, single-arm, phase 3 trials (one at 15 US academic and community sites and one at 12 US and international academic and community sites), participants followed a 21-days-in, 7-days-out segesterone acetate and ethinylestradiol contraceptive vaginal system schedule for up to 13 cycles. Participants were healthy, sexually active, non-pregnant, non-sterilised women aged 18–40 years. Women were cautioned that any removals during the 21 days of cyclic use should not exceed 2 h, and used daily paper diaries to record vaginal system use. Consistent with regulatory requirements for contraceptives, we calculated the Pearl Index for women aged 35 years and younger, excluding adjunctive contraception cycles, as the primary efficacy outcome measure. We also did intention-to-treat Kaplan-Meier life table analyses and followed up women who did not use hormonal contraceptives or desired pregnancy after study completion for 6 months for return to menses or pregnancy. The trials are registered with ClinicalTrials.gov, numbers NCT00455156 and NCT00263341. Findings: Between Dec 19, 2006, and Oct 9, 2009, at the 15 US sites, and between Nov 1, 2006, and July 2, 2009, at the 12 US and international sites we enrolled 2278 women. Our overall efficacy analysis included 2265 participants (1130 in the US study and 1135 in the international study) and 1303 (57·5%) participants completed up to 13 cycles. The Pearl Index for the primary efficacy group was 2·98 (95% CI 2·13–4·06) per 100 woman-years, and was well within the range indicative of efficacy for a contraceptive under a woman's control. The Kaplan-Meier analysis revealed the contraceptive vaginal system was 97·5% effective, which provided further evidence of efficacy. Pregnancy occurrence was similar across cycles. All 290 follow-up participants reported return to menses or became pregnant (24 [63%] of 38 women who desired pregnancy) within 6 months. Interpretation: The segesterone acetate and ethinylestradiol contraceptive vaginal system is an effective contraceptive for 13 consecutive cycles of use. This new product adds to the contraceptive method mix and the 1-year duration of use means that women do not need to return to the clinic or pharmacy for refills every few months. Funding: Eunice Kennedy Shriver National Institute of Child Health and Human Development of the National Institutes of Health, the US Agency for International Development, and the WHO Reproductive Health Research Department.
AB - Background: A ring-shaped, contraceptive vaginal system designed to last 1 year (13 cycles) delivers an average of 0·15 mg segesterone acetate and 0·013 mg ethinylestradiol per day. We evaluated the efficacy of this contraceptive vaginal system and return to menses or pregnancy after use. Methods: In two identically designed, multicentre, open-label, single-arm, phase 3 trials (one at 15 US academic and community sites and one at 12 US and international academic and community sites), participants followed a 21-days-in, 7-days-out segesterone acetate and ethinylestradiol contraceptive vaginal system schedule for up to 13 cycles. Participants were healthy, sexually active, non-pregnant, non-sterilised women aged 18–40 years. Women were cautioned that any removals during the 21 days of cyclic use should not exceed 2 h, and used daily paper diaries to record vaginal system use. Consistent with regulatory requirements for contraceptives, we calculated the Pearl Index for women aged 35 years and younger, excluding adjunctive contraception cycles, as the primary efficacy outcome measure. We also did intention-to-treat Kaplan-Meier life table analyses and followed up women who did not use hormonal contraceptives or desired pregnancy after study completion for 6 months for return to menses or pregnancy. The trials are registered with ClinicalTrials.gov, numbers NCT00455156 and NCT00263341. Findings: Between Dec 19, 2006, and Oct 9, 2009, at the 15 US sites, and between Nov 1, 2006, and July 2, 2009, at the 12 US and international sites we enrolled 2278 women. Our overall efficacy analysis included 2265 participants (1130 in the US study and 1135 in the international study) and 1303 (57·5%) participants completed up to 13 cycles. The Pearl Index for the primary efficacy group was 2·98 (95% CI 2·13–4·06) per 100 woman-years, and was well within the range indicative of efficacy for a contraceptive under a woman's control. The Kaplan-Meier analysis revealed the contraceptive vaginal system was 97·5% effective, which provided further evidence of efficacy. Pregnancy occurrence was similar across cycles. All 290 follow-up participants reported return to menses or became pregnant (24 [63%] of 38 women who desired pregnancy) within 6 months. Interpretation: The segesterone acetate and ethinylestradiol contraceptive vaginal system is an effective contraceptive for 13 consecutive cycles of use. This new product adds to the contraceptive method mix and the 1-year duration of use means that women do not need to return to the clinic or pharmacy for refills every few months. Funding: Eunice Kennedy Shriver National Institute of Child Health and Human Development of the National Institutes of Health, the US Agency for International Development, and the WHO Reproductive Health Research Department.
UR - http://www.scopus.com/inward/record.url?scp=85068566005&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85068566005&partnerID=8YFLogxK
U2 - 10.1016/S2214-109X(19)30265-7
DO - 10.1016/S2214-109X(19)30265-7
M3 - Article
C2 - 31231065
AN - SCOPUS:85068566005
SN - 2214-109X
VL - 7
SP - e1054-e1064
JO - The Lancet Global Health
JF - The Lancet Global Health
IS - 8
ER -