4.3 Article

Therapeutically equivalent pharmacokinetic profile across three application sites for AG200-15, a novel low-estrogen dose contraceptive patch

Journal

CONTRACEPTION
Volume 87, Issue 6, Pages 744-749

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.contraception.2012.10.038

Keywords

Contraception; Patch; Anatomical sites; Pharmacokinetic; Ethinyl estradiol; Levonorgestrel

Funding

  1. Agile Therapeutics, Inc.

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Background: AG200-15 Agile Patch (AP) is a novel 7-day contraceptive patch providing ethinyl estradiol (EE) exposure comparable to low-dose combination oral contraceptives. This study determined whether application of the AP to three different anatomical sites (lower abdomen, buttock and upper torso) influences the pharmacokinetic profile of EE and levonorgestrel (LNG). Study Design: In this open-label, three-period, crossover study, 24 subjects were randomized to one of six treatment sequences; each included application of patch to abdomen, buttock and upper torso, with the AP worn on one site for 7 days. After a 7-day washout, a new patch was applied to the next anatomical site. Multiple blood samples were collected up to 240 h after patch application. Results: For plasma EE levels, median time to maximum drug concentration (T-max, 24-48 h) and mean maximum concentration (C-max, 47.9-61.5 pg/mL) were similar among application sites. Compared with lower abdomen, EE exposure was higher (16%-30%) at buttock and upper torso (15%-22%). For plasma LNG levels, median T-max, (72-120 h) and mean C-max (1436-1589 pg/mL) were similar across application sites. Compared with lower abdomen, LNG exposure was higher at buttock (1%-7%) and upper torso (16%-17%). No serious adverse events (AEs) or AE-related discontinuations occurred. The most common treatment-emergent AEs were nausea, application site pruritus and headache, with frequencies comparable across anatomical sites. Conclusions: Absorption from the abdomen was slightly lower versus other sites; however, exposure to EE and LNG for all sites was therapeutically equivalent. The AP was well tolerated at all three anatomical sites. (C) 2013 Elsevier Inc. All rights reserved.

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