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PMID: 2142930 Published · ppublish English Clinical Trial Comparative Study Controlled Clinical Trial Journal Article

Relative bioavailability of ethinyl estradiol from two different oral contraceptive formulations after single oral administration to 18 women in an intraindividual cross-over design.

Hormone research ·Vol. 33 ·No. 1 ·1990-00-00 ·Pages 40-4

Kuhnz W, Hümpel M, Schütt B, Louton T, Steinberg B, Gansau C

Abstract

Two low-dose oral contraceptives, both containing the same dose of ethinyl estradiol (EE2) but different progestins (gestodene and desogestrel, respectively), were compared with respect to the relative bioavailability of EE2. After single-dose administration of both formulations to 18 women in an intraindividual cross-over design, there was no difference in the target variables for EE2 (Cmax, tmax and AUC). With respect to EE2, both formulations were bioequivalent. The observation of others, reporting higher EE2 levels in the serum of women taking the gestodene-containing formulation as compared to those taking the desogestrel-containing formulation, was not confirmed.

MeSH Terms
Adult Biological Availability Chemistry, Pharmaceutical Contraceptives, Oral/administration & dosage Desogestrel Drug Administration Schedule Drug Combinations Ethinyl Estradiol/blood,pharmacokinetics Female Humans Norpregnenes/pharmacokinetics Random Allocation
Chemicals
Contraceptives, Oral Drug Combinations Norpregnenes Gestodene Ethinyl Estradiol Desogestrel
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kuhnz W
Schering AG Research Laboratories, Berlin/Bergkamen.
Hümpel M
Schütt B
Louton T
Steinberg B
Gansau C
Article Info
Journal
Hormone research
Abbr.
Horm Res
ISSN
0301-0163
Published
1990-00-00
Pages
40-4
Language
English
Region
Switzerland
NLM ID
0366126
Subset
IM
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