Estetrol-Drospirenone combination oral contraceptive: a clinical study of contraceptive efficacy, bleeding pattern and safety in Europe and Russia.
Bleeding pattern
combined oral contraception
contraceptive efficacy
drospirenone
estetrol
native estrogen
safety
Journal
BJOG : an international journal of obstetrics and gynaecology
ISSN: 1471-0528
Titre abrégé: BJOG
Pays: England
ID NLM: 100935741
Informations de publication
Date de publication:
Jan 2022
Jan 2022
Historique:
revised:
03
05
2021
received:
27
01
2021
accepted:
20
05
2021
pubmed:
11
7
2021
medline:
22
1
2022
entrez:
10
7
2021
Statut:
ppublish
Résumé
To assess the contraceptive efficacy, bleeding pattern and safety of a combined oral contraceptive containing estetrol (E4) 15 mg and drospirenone (DRSP) 3 mg. Multicenter, open-label, phase 3 trial. Sixty-nine sites in Europe and Russia. Sexually active women aged 18-50 years with regular menstrual cycles and body mass index ≤35 kg/m E4/DRSP was administered in a 24 active/4 placebo regimen for up to 13 cycles. Visits were scheduled during Cycles 2, 4, 7 and 10 and after completing treatment during which adverse events (AEs) were collected. Participants recorded medication intake, vaginal bleeding/spotting, use of other contraceptive methods and sexual intercourse on a daily diary. Pearl Index (PI) for women 18-35 years (overall and method-failure), bleeding pattern and AEs. A total of 1553 women aged 18-50 years, including 1353 from 18 to 35 years old, received the study medication. PI was 0.47 pregnancies/100 woman-years (95% CI 0.15-1.11); method failure PI was 0.29 pregnancies/100 woman-years (95% CI 0.06-0.83). Scheduled bleeding/spotting occurred in 91.9-94.4% of women over Cycles 1 to 12 and lasted a median of 4-5 days per cycle. The percentage of women with unscheduled bleeding/spotting episodes decreased from 23.5% in Cycle 1 to <16% from Cycle 6 onwards. The most common AEs were headache (7.7%), metrorrhagia (5.5%), vaginal haemorrhage (4.8%) and acne (4.2%). One treatment-related serious AE was reported, a lower extremity venous thromboembolism. One-hundred and forty-one (9.1%) women discontinued study participation because of treatment-related adverse events. E4/DRSP provides effective contraception, a predictable bleeding pattern and a favourable safety profile. A phase 3 trial with E4/DRSP shows high contraceptive efficacy, a predictable bleeding pattern and favourable safety profile.
Identifiants
pubmed: 34245666
doi: 10.1111/1471-0528.16840
pmc: PMC9290720
doi:
Substances chimiques
Contraceptives, Oral, Combined
0
drospirenone and estetrol
0
Estetrol
ENB39R14VF
Types de publication
Clinical Trial, Phase III
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
63-71Subventions
Organisme : Estetra SRL, an affiliate company of Mithra Pharmaceuticals
ID : n/a
Informations de copyright
© 2021 Estetra SRL. BJOG: An International Journal of Obstetrics and Gynaecology published by John Wiley & Sons Ltd.
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