An intravaginal ring for real-time evaluation of adherence to therapy

Two recent Phase III clinical trials to investigate an intravaginal ring for preventing HIV infection demonstrated that adherence to prescribed device use was a primary driver of efficacy. Surrogate methods for determining adherence in the studies were limited in their inability to monitor temporal...

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Published inPloS one Vol. 12; no. 4; p. e0174729
Main Authors Moss, John A, Baum, Marc M, Easley, Jeremiah T, Cox, Darren M, Smith, Thomas J
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 06.04.2017
Public Library of Science (PLoS)
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Summary:Two recent Phase III clinical trials to investigate an intravaginal ring for preventing HIV infection demonstrated that adherence to prescribed device use was a primary driver of efficacy. Surrogate methods for determining adherence in the studies were limited in their inability to monitor temporal patterns of use and allow deconvolution of the effects of adherence and device efficacy on HIV infection rates. To address this issue, we have developed functionality in an intravaginal ring to continuously monitor when the device is being used and maintain a log of adherence that can be accessed by clinicians after it is removed. An electronic module fabricated with common, inexpensive electronic components was encapsulated in a silicone intravaginal ring. The device uses temperature as a surrogate measure of periods of device insertion and removal, and stores a record of the data for subsequent retrieval. The adherence-monitoring intravaginal ring accurately recorded the device status over 33 simulated IN-OUT cycles and more than 1000 measurement cycles in vitro. Following initial in vitro testing in a temperature-controlled chamber, the device was evaluated in vivo in sheep using a predetermined insertion/removal pattern to simulate intravaginal ring use. After insertion into the vaginal cavity of a sheep, the logged data correctly indicated the device status over 29 hours of continuous measurement including three cycles of insertion and removal. The device described here is a promising, low-cost method for real-time adherence assessment in clinical trials involving medicated intravaginal rings or other intravaginal devices.
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Competing Interests: JM and MB are employees of Oak Crest Institute of Science, a non-profit research institute; DC is an independent consultant paid by Oak Crest for work on device electronics design and programming; JE is an employee of Colorado State University. TS is an employee and CEO of Auritec Pharmaceuticals, a for-profit pharmaceutical company. This does not alter our adherence to PLOS ONE policies on sharing data and materials. There are no additional known conflicts of interest.
Conceptualization: JM MB TS.Data curation: JM DC.Formal analysis: JM.Funding acquisition: JM TS.Investigation: JM JE.Methodology: JM JE.Project administration: JM.Resources: JM DC JE.Software: JM DC.Supervision: JM.Validation: JM.Visualization: JM.Writing – original draft: JM.Writing – review & editing: JM MB JE.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0174729