TY - JOUR
T1 - Effect of double-dose levonorgestrel subdermal implant in women taking efavirenz-based antiretroviral therapy
T2 - The DoubLNG pharmacokinetic study
AU - Cirrincione, Lauren R.
AU - Nakalema, Shadia
AU - Chappell, Catherine A.
AU - Byakika-Kibwika, Pauline
AU - Kyohairwe, Isabella
AU - Winchester, Lee
AU - Mackline, Hope
AU - Pham, Michelle M.
AU - Cohn, Susan E.
AU - Siccardi, Marco
AU - Owen, Andrew
AU - Fletcher, Courtney V.
AU - Lamorde, Mohammed
AU - Scarsi, Kimberly K.
N1 - Funding Information:
Funding: This work was supported by the Eunice Kennedy Shrive National Institute of Child Health and Human Development (grant number R01 HD085887 to KS). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The funder had no role in the conduct, analyses, and conclusions of the study. The corresponding author had full access to all study data and had final responsibility for the decision to submit for publication.
Funding Information:
Funding: This work was supported by the Eunice Kennedy Shrive National Institute of Child Health and Human Development (grant number R01 HD085887 to KS). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The funder had no role in the conduct, analyses, and conclusions of the study. The corresponding author had full access to all study data and had final responsibility for the decision to submit for publication.
Publisher Copyright:
© 2023 The Author(s)
PY - 2023/6
Y1 - 2023/6
N2 - Objective: We evaluated the pharmacokinetics of double-dose levonorgestrel (LNG) implants to overcome the drug–drug interaction with efavirenz-based antiretroviral therapy (ART). Study design: We conducted a nonrandomized, open-label, parallel-group, longitudinal pharmacokinetic study among Ugandan women ages 18–45 years. Participants with HIV on ART containing efavirenz 600 mg received 300 mg of LNG implants (Jadelle®, Bayer, New Zealand): 300LNG+ART group. We compared our outcomes with women without HIV using standard dose, 150 mg of LNG implants: 150LNG group. The implant was placed on day zero in both groups, and we quantified plasma LNG concentrations over 48 weeks post implant insertion. LNG pharmacokinetic parameters were estimated using noncompartmental techniques. Our primary outcome was the geometric mean ratio with 90% confidence intervals of LNG area under the concentration–time curve over 24 weeks (AUC0–24w) between groups. Demographic data were described as median (interquartile range). A secondary outcome compared between-group percent of LNG concentrations ≥300 pg/mL, a minimum threshold selected a priori based on observed pregnancies in Ugandan women on standard-dose LNG implants plus efavirenz. Results: We enrolled 27 women in the 300LNG+ART group (34 [28.0 to 40.5] years and 61.0 [49.8–66.0] kg) and 19 women in the 150LNG group (33 [30.0 to 34.5] years and 64.9 [59.0 to 74.5] kg). LNG AUC0–24w was 34% lower for 300LNG+ART versus 150LNG (geometric mean 9998 vs. 15,231 pg*week/mL, respectively [geometric mean ratio 0.66 (90% confidence intervals, 0.54 to 0.80)]). The percentage of participants with LNG concentrations ≥300 pg/mL was not statistically different between groups at week 24 (300LNG+ART: 74.1%; 150LNG: 89.5%; p = 0.27). Conclusion: Double-dose LNG implant did not completely overcome the drug–drug interaction with efavirenz. Implication: In women using ART containing efavirenz, placing two implant systems (300 mg) did not normalize LNG pharmacokinetics compared with the standard-dose implant (150 mg), and some women had evidence of ovulatory activity. Alternative ART without drug–drug interactions, such as dolutegravir, is recommended with contraceptive implants.
AB - Objective: We evaluated the pharmacokinetics of double-dose levonorgestrel (LNG) implants to overcome the drug–drug interaction with efavirenz-based antiretroviral therapy (ART). Study design: We conducted a nonrandomized, open-label, parallel-group, longitudinal pharmacokinetic study among Ugandan women ages 18–45 years. Participants with HIV on ART containing efavirenz 600 mg received 300 mg of LNG implants (Jadelle®, Bayer, New Zealand): 300LNG+ART group. We compared our outcomes with women without HIV using standard dose, 150 mg of LNG implants: 150LNG group. The implant was placed on day zero in both groups, and we quantified plasma LNG concentrations over 48 weeks post implant insertion. LNG pharmacokinetic parameters were estimated using noncompartmental techniques. Our primary outcome was the geometric mean ratio with 90% confidence intervals of LNG area under the concentration–time curve over 24 weeks (AUC0–24w) between groups. Demographic data were described as median (interquartile range). A secondary outcome compared between-group percent of LNG concentrations ≥300 pg/mL, a minimum threshold selected a priori based on observed pregnancies in Ugandan women on standard-dose LNG implants plus efavirenz. Results: We enrolled 27 women in the 300LNG+ART group (34 [28.0 to 40.5] years and 61.0 [49.8–66.0] kg) and 19 women in the 150LNG group (33 [30.0 to 34.5] years and 64.9 [59.0 to 74.5] kg). LNG AUC0–24w was 34% lower for 300LNG+ART versus 150LNG (geometric mean 9998 vs. 15,231 pg*week/mL, respectively [geometric mean ratio 0.66 (90% confidence intervals, 0.54 to 0.80)]). The percentage of participants with LNG concentrations ≥300 pg/mL was not statistically different between groups at week 24 (300LNG+ART: 74.1%; 150LNG: 89.5%; p = 0.27). Conclusion: Double-dose LNG implant did not completely overcome the drug–drug interaction with efavirenz. Implication: In women using ART containing efavirenz, placing two implant systems (300 mg) did not normalize LNG pharmacokinetics compared with the standard-dose implant (150 mg), and some women had evidence of ovulatory activity. Alternative ART without drug–drug interactions, such as dolutegravir, is recommended with contraceptive implants.
KW - Drug interactions
KW - Efavirenz
KW - HIV
KW - Levonorgestrel
KW - Long-acting reversible contraceptives
KW - Pharmacokinetics
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U2 - 10.1016/j.contraception.2023.109975
DO - 10.1016/j.contraception.2023.109975
M3 - Article
C2 - 36787829
AN - SCOPUS:85150387192
SN - 0010-7824
VL - 122
JO - Contraception
JF - Contraception
M1 - 109975
ER -