Suppression of ovulation and pharmacokinetics following subcutaneous administration of various doses of Depo-Provera®: a randomized trial

Objectives: To identify the lowest dose of Depo-Provera that, when administered off-label subcutaneously, suppressed ovulation and had a pharmacokinetic profile consistent with a 4-month contraceptive effect.Study Design: We conducted a randomized, multicenter, parallel-group study to evaluate the p...

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Main Authors: Vera Halpern (Author), Rachael Fuchs (Author), Vivian Brache (Author), Luis Bahamondes (Author), Maria Jose Miranda (Author), Anja Lendvay (Author), Leila Cochón (Author), Douglas Taylor (Author), Laneta J. Dorflinger (Author)
Format: Book
Published: Elsevier, 2021-01-01T00:00:00Z.
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001 doaj_52a60f16f00c44a0b05c536e40d343dd
042 |a dc 
100 1 0 |a Vera Halpern  |e author 
700 1 0 |a Rachael Fuchs  |e author 
700 1 0 |a Vivian Brache  |e author 
700 1 0 |a Luis Bahamondes  |e author 
700 1 0 |a Maria Jose Miranda  |e author 
700 1 0 |a Anja Lendvay  |e author 
700 1 0 |a Leila Cochón  |e author 
700 1 0 |a Douglas Taylor  |e author 
700 1 0 |a Laneta J. Dorflinger  |e author 
245 0 0 |a Suppression of ovulation and pharmacokinetics following subcutaneous administration of various doses of Depo-Provera®: a randomized trial 
260 |b Elsevier,   |c 2021-01-01T00:00:00Z. 
500 |a 2590-1516 
500 |a 10.1016/j.conx.2021.100070 
520 |a Objectives: To identify the lowest dose of Depo-Provera that, when administered off-label subcutaneously, suppressed ovulation and had a pharmacokinetic profile consistent with a 4-month contraceptive effect.Study Design: We conducted a randomized, multicenter, parallel-group study to evaluate the pharmacokinetics (PK) and pharmacodynamics (PD) of medroxyprogesterone acetate (MPA) after subcutaneous injection of three different doses of Depo-Provera. We randomized sixty women between 18 and 40 years of age at low risk of pregnancy with confirmed ovulation and body mass index of 18 to 35 kg/m2 to receive a single injection of 45, 75 or 105 mg of Depo-Provera, or a single injection of Depo-subQ provera 104 as a reference drug (15 women per group) and followed them for 7.5 months. We evaluated suppression of ovulation as the primary outcome, and MPA concentrations, pharmacokinetic parameters, safety, and local tolerability as secondary outcomes.Results: Five women ovulated within four months of treatment initiation (three in the 45 mg group and two in the 75 mg group). MPA levels associated with ovulation were in general low, largely ≤ 0.2 ng/mL (the presumed contraceptive threshold). No women in either the 105 mg group or the Depo-subQ provera 104 group ovulated within four months. The PK parameters including Cmax, C119, and AUC0−119 for these 2 groups were similar but not equivalent.Conclusion: A dose of 105 mg of Depo-Provera injected subcutaneously was the lowest tested dose that consistently suppressed ovulation and maintained serum MPA levels consistent with contraceptive effect for at least 4 months. The PK and PD results for the 105 mg dose were similar to Depo-subQ provera 104 over this period. 
546 |a EN 
690 |a Contraception 
690 |a Depot medroxyprogesterone acetate 
690 |a Depo-provera 
690 |a Ovulation 
690 |a Pharmacokinetics 
690 |a Subcutaneous 
690 |a Gynecology and obstetrics 
690 |a RG1-991 
690 |a Public aspects of medicine 
690 |a RA1-1270 
655 7 |a article  |2 local 
786 0 |n Contraception: X, Vol 3, Iss , Pp 100070- (2021) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S2590151621000174 
787 0 |n https://doaj.org/toc/2590-1516 
856 4 1 |u https://doaj.org/article/52a60f16f00c44a0b05c536e40d343dd  |z Connect to this object online.