Contraception
Volume 82, Issue 4 , Pages 358-365, October 2010

Endometrial safety of a novel monophasic combined oral contraceptive containing 0.02 mg ethinylestradiol and 2 mg chlormadinone acetate administered in a 24/4-day regimen over six cycles

  • Thomas Rabe

      Affiliations

    • University Women's Hospital, Voß-Str. 9, D-69115 Heidelberg, Germany
    • Corresponding Author InformationCorresponding author. Tel.: +49 6221 567913; fax: +49 6221 560713.
  • ,
  • Elena Hartschuh

      Affiliations

    • Neuenheimer Landstr. 60, D-69120 Heidelberg, Germany
  • ,
  • Torsten Wahlstrom

      Affiliations

    • Laboratory of Pathology, Eira Hospital, Tehtaan Katu 28, SF-00150 Helsinki, Finland
  • ,
  • Kornelia Höschen

      Affiliations

    • Grunenthal GmbH, D-52099 Aachen, Germany
  • ,
  • Simone König

      Affiliations

    • Grunenthal GmbH, D-52099 Aachen, Germany

Received 18 September 2009; received in revised form 13 April 2010; accepted 14 April 2010. published online 12 July 2010.

Abstract 

Background

This study was conducted to examine whether small doses of ethinylestradiol (EE, 0.02 mg) and chlormadinone acetate (CMA, 2 mg) administered in a novel 24/4-day regimen during six cycles would suffice to suppress proliferation and to cause secretory changes in the endometrium.

Study Design

This Phase II, randomized (two assessment groups), single-center, open, uncontrolled, multiple-dosing study treated 59 female subjects. The subjects underwent three endometrial biopsies: one pretreatment, one during medication (either at Cycle 3 or Cycle 6) and one during the first post-treatment cycle.

Results

The study revealed that 0.02 mg EE/2 mg CMA effectively transformed the endometrium from a proliferative state into a secretory or inactive state after three (90% of subjects) and six (76% of subjects) medication cycles. The mean endometrial thickness decreased markedly from 10.2 (SD±3.0) mm (pretreatment) to an unfavorable level for the nidation of a blastocyst [5.3 (SD±2.1) and 4.1 (SD±2.2) mm in Medication Cycles 3 and 6, respectively]. Correspondingly, estradiol and progesterone levels decreased during treatment.

In the post-treatment cycle, endometrial biopsy and ultrasound evaluation as well as sex hormone levels suggested a quick return to fertility. There were no signs of hyperplasia, endometrial polyps, neoplasia or other detrimental histopathological changes at any time during the trial. Treatment-related adverse events (AEs) were reported by 22 (37%) of 59 subjects and were reported most commonly in Cycle 1, decreasing continuously thereafter. No AEs led to discontinuation of the trial medication and there were no serious AEs.

Conclusions

The 24/4-day regimen of 0.02 mg EE/2 mg CMA provided effective and reversible endometrial effects with secretory transformation or suppression without inducing pathological changes.

Keywords: Oral contraception, Combined oral contraceptive, Chlormadinone acetate, Low-dose ethinylestradiol, 24/4-day regimen, Endometrium

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PII: S0010-7824(10)00150-2

doi:10.1016/j.contraception.2010.04.013

Contraception
Volume 82, Issue 4 , Pages 358-365, October 2010