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Early Phase 1 N=14 Randomized Single-blind Diagnostic

Project ADHERE: Clinical Proof-of-Concept of a Tenofovir (TFV) Aptamer-Based Biosensor

HIV/AIDS · Adherence, Medication · Drug Use

Enrolled (actual)
14
Serious AEs
0.0%
Results posted
Jan 2024
Primary outcome: Primary: Baseline TFV (Tenofovir) Levels in Plasma

Study Design & Population

Study type
Interventional
Phase
Early Phase 1
Interventions
Tenofovir Disoproxil Fumarate/Emtricitabine (TDF/FTC) (Drug)
Age
Adult · 18+ yrs
Sex
Female
Sponsor
Eastern Virginia Medical School
Primary completion
Jan 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Baseline TFV (Tenofovir) Levels in Plasma
PRIMARY
Levels of TFV in Plasma After Different Lengths of Time Post-first Dose
PRIMARY
Levels of TFV in Plasma After Different Lengths of Time Post-first Dose
PRIMARY
Levels of TFV in Plasma After Different Lengths of Time Post-first Dose

Summary

Truvada®, an oral pill comprised of two anti-retroviral compounds, emtricitabine (FTC) and tenofovir disoproxil fumarate (TDF), is currently the only drug combination approved for pre-exposure prophylaxis (PrEP) in women exposed to high HIV risk through vaginal acquisition. Adherence to the one pill per day regimen is crucial for its effectiveness in reducing the risk of acquiring HIV. Currently, there is no available point of care diagnostic test to quickly measure blood levels of tenofovir in the clinic. This study will determine whether a tenofovir (TFV) aptamer-based biosensor (aptasensor) can detect TFV in biological fluids from women randomized to different dosing regimens representing high and low adherence.

Eligibility Criteria

Inclusion Criteria

  • Age 18 to 50 years, inclusive
  • General good health (by volunteer history and per investigator judgment) without any clinically significant systemic disease (including, but not limited to significant liver disease/hepatitis, gastrointestinal disease, kidney disease, thyroid disease, osteoporosis or bone disease, and diabetes) and with an intact gastrointestinal tract, uterus and cervix.
  • Estimated calculated creatinine clearance (eCcr) of at least 80 mL/min
  • Body Mass Index (BMI) of ≥18 and 45 kg (99.2 lbs)
  • Willing to give voluntary consent and sign an informed consent form
  • Willing and able to comply with protocol requirements, including swallowing tablets
  • Must be protected from pregnancy by:
  • Condoms
  • Hormonal contraceptives
  • Copper or Levonorgestrel intrauterine device (IUD)
  • Sterilization of either partner
  • Heterosexual abstinence
  • Same sex relationship
  • If in a relationship, must be in a mutually monogamous relationship with a partner who is not known to be HIV positive and has no known risk of STIs

Exclusion Criteria

  • Currently pregnant
  • Currently breastfeeding or planning to breastfeed during the course of the study
  • In the last three months, diagnosed with or treated for any STI
  • Positive test for HIV, or Hepatitis B surface antigen (HBsAg)
  • Systemic use in the last two weeks or anticipated use during the study of any of the following: antiretrovirals (e.g. Viread®, Atripla®, Emtriva®, or Complera®), or drugs that may interact with TFV (e.g., protease inhibitors, anticonvulsants, antimycobacterials, St. John's Wort).
  • Participation in any other investigational trial with use of a drug/device within the last 30 days or planned participation in any other investigational trial with use of a drug/device during the study
  • Grade 2 or higher laboratory abnormality, per the 2014 update of the Division of AIDS, National Institute of Allergy and Infectious Disease (DAIDS) Table for Grading the Severity of Adverse Events, or clinically significant laboratory abnormality as determined by the clinician
  • Abnormal finding on laboratory or physical examination or a social or medical condition in the volunteer which, in the opinion of the investigator, would make participation in the study unsafe or would complicate interpretation of data
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04870671). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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