The addition of a short- or medium-acting estrogen ester to the long-a
cting progestins depot-medroxygrogesterone acetate (DMPA) and norethis
terone enanthate (NET-EN) to produce ''combined'' injectable formulati
ons has proved a successful strategy in the development of once-a-mont
h injectable contraceptives. Recent clinical pharmacokinetic studies u
ndertaken on once-a-month injectable contraceptives in various WHO Col
laborating Centers have guided the selection of the estrogen-progestog
en combinations, ratios and dose schedules. At least three combined on
ce-a-month injectable preparations exhibit acceptable pharmacokinetic
and pharmacodynamic profiles; however, further improvement in the desi
gn of optimal estrogen/progestin injectables are expected during this
decade