Your browser doesn't support javascript.
loading
Phase 1 randomized trials to assess safety, pharmacokinetics, and vaginal bleeding associated with use of extended duration dapivirine and levonorgestrel vaginal rings.
Achilles, Sharon L; Kelly, Clifton W; Hoesley, Craig J; Blithe, Diana L; Brown, Jill; Richardson, Barbra A; Devlin, Brid; Hendrix, Craig W; Poloyac, Samuel M; Marzinke, Mark A; Gundacker, Holly; Singh, Devika; Piper, Jeanna M; Johnson, Sherri; Steytler, John; Chen, Beatrice A.
Afiliação
  • Achilles SL; Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Kelly CW; Magee-Womens Research Institute, Pittsburgh, Pennsylvania, United States of America.
  • Hoesley CJ; Statistical Center for HIV/AIDS Research & Prevention, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
  • Blithe DL; University of Alabama at Birmingham Heersink School of Medicine, Birmingham, Alabama, United States of America.
  • Brown J; National Institute of Child Health and Human Development, Contraceptive Development Program, DIPHR, NIH, Bethesda, Maryland, United States of America.
  • Richardson BA; National Institute of Child Health and Human Development, Contraceptive Development Program, DIPHR, NIH, Bethesda, Maryland, United States of America.
  • Devlin B; Statistical Center for HIV/AIDS Research & Prevention, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
  • Hendrix CW; Department of Biostatistics, University of Washington, Seattle, Washington, United States of America.
  • Poloyac SM; International Partnership for Microbicides, Silver Spring, Maryland, United States of America.
  • Marzinke MA; Department of Medicine, Division of Clinical Pharmacology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
  • Gundacker H; Department of Pharmaceutical Sciences, School of Pharmacy, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Singh D; Department of Medicine, Division of Clinical Pharmacology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
  • Piper JM; Statistical Center for HIV/AIDS Research & Prevention, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
  • Johnson S; Magee-Womens Research Institute, Pittsburgh, Pennsylvania, United States of America.
  • Steytler J; National Institutes of Allergy and Infectious Disease, NIH, Bethesda, Maryland.
  • Chen BA; FHI 360, Durham, North Carolina, United States of America.
PLoS One ; 19(6): e0304552, 2024.
Article em En | MEDLINE | ID: mdl-38838028
ABSTRACT

BACKGROUND:

Vaginal rings formulated to deliver two drugs simultaneously have potential as user-controlled, long-acting methods for dual prevention of HIV and pregnancy.

METHODS:

Two phase 1 randomized trials (MTN-030/IPM 041 and MTN-044/IPM 053/CCN019) respectively enrolled 24 and 25 healthy, HIV-negative participants to evaluate safety, pharmacokinetics, and vaginal bleeding associated with use of a vaginal ring containing 200mg dapivirine (DPV) and 320mg levonorgestrel (LNG) designed for 90-day use. MTN-030/IPM 041 compared the DPV/LNG ring to a DPV-only ring (200mg) over 14 days of use. MTN-044/IPM 053/CCN019 compared continuous or cyclic use of the DPV/LNG ring over 90 days of use. Safety was assessed by recording adverse events (AEs). DPV and LNG concentrations were quantified in plasma, cervicovaginal fluid, and cervical tissue. Vaginal bleeding was self-reported.

RESULTS:

There were no differences in the proportion of participants with grade ≥2 genitourinary AEs or grade ≥3 AEs with DPV/LNG ring vs. DPV ring use (p = .22), or with DPV/LNG ring continuous vs. cyclic use (p = .67). Higher plasma DPV concentrations were observed in users of DPV/LNG compared to DPV-only rings (Cmax p = 0.049; AUC p = 0.091). Plasma DPV and LNG concentrations were comparable with continuous and cyclic use (Cmax p = 0.74; AUC p = 0.25). With cyclic use, median nadir plasma DPV concentration was approximately 300 pg/mL two days after removal and median t1/2 for cervicovaginal fluid DPV concentration was 5.76 hours (n = 3). Overall bleeding experiences did not differ between continuous and cyclic users (p = 0.12).

CONCLUSIONS:

The extended duration DPV/ LNG rings were well tolerated and the observed DPV concentrations in plasma and cervicovaginal fluid when used continuously exceeded concentrations observed in previous DPV ring efficacy studies. LNG concentrations in plasma were comparable with other efficacious LNG-based contraceptives. Genital DPV concentrations had a short half-life and were thus not well sustained following ring removal.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirimidinas / Hemorragia Uterina / Levanogestrel / Dispositivos Anticoncepcionais Femininos Limite: Adult / Female / Humans / Middle aged Idioma: En Revista: PLoS One Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirimidinas / Hemorragia Uterina / Levanogestrel / Dispositivos Anticoncepcionais Femininos Limite: Adult / Female / Humans / Middle aged Idioma: En Revista: PLoS One Ano de publicação: 2024 Tipo de documento: Article