Phase 1 Safety and Pharmacokinetic Study of Polyurethane Tenofovir Disoproxil Fumarate Vaginal Ring
Trial Snapshot
- Phase
- Phase 1
- Status
- Completed
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Grade 1 Genitourinary Events or Higher as Defined by the DAIDS Table for Grading the Severity of Adult and Pediatric Adverse Events
Study Overview
Brief Summary
This prospective, randomized, single-blinded, placebo controlled trial will examine the safety and pharmacokinetics (PK) of a polyurethane tenofovir disoproxil fumarate (TDF) vaginal ring when used continuously for 14 consecutive days.
The primary objective is to assess the safety of TDF vaginal rings when used continuously for 14 days by healthy, HIV-uninfected, sexually abstinent women, as compared with a placebo vaginal ring.
Detailed Description
Tenofovir disoproxil fumarate (TDF) is a prodrug of TFV (tenofovir), an adenosine nucleoside monophosphonate (nucleotide) derivative with potent antiretroviral (ARV) activity. TDF permeates cells more rapidly than TFV resulting in increased intracellular accumulation of TFV-diphosphate (TFV-DP), the active metabolite. TDF is more potent than TFV and inhibits HIV-1 (Human Immunodeficiency Virus-1)and herpes simplex virus type 2 (HSV-2) infection in cell and tissue culture models at approximately 100-fold lower concentrations than TFV, suggesting that it may be an excellent candidate for prevention of HIV. TDF is licensed for the treatment of HIV-1 infection in the US, the European Union, Middle East, and Africa.
The study will take place at the Albert Einstein College of Medicine in Bronx, New York, USA. Each participant will receive an IVR (intravaginal ring) containing TDF or a placebo ring. The vaginal ring will be worn continuously for 14 days. It will be inserted into the vagina following cessation of participant's menses, by the study clinician at Visit 3 and removed by the study clinician at Visit 7. Each participant will be followed for 7 days following ring removal.
It is hypothesized that both the TDF IVR and placebo IVR will be safe and well tolerated among healthy, sexually abstinent women on combined-hormonal contraception. The null hypothesis is that there will be no difference in the safety profile between the active product and the placebo.
Careful assessments of safety, including systemic and genital tract, will be undertaken with special consideration for issues related to irritation and systemic toxicity. The design of the study will allow safety comparisons of TDF ring to a placebo ring. A 14-day safety and PK study is proposed for this first-in-human study per FDA (For and Drug Administration) guidance. The study duration was carefully selected to control risk to the study participants. TFV 1% vaginal gel has been extensively tested in clinical trials at higher doses (8-fold dose margin) than the predicted dose delivered by the TDF IVR-001 study, and the TFV gel showed no significant adverse events at this higher dose in thousands of women.
Given the drug release kinetics observed in vitro and in NHP (non-human primate) studies, TDF and TFV (formed following hydrolysis of the prodrug TDF) concentrations in cervicovaginal fluid (CVF) are expected to reach steady state within a few days and maintain steady state concentrations for the duration of the planned 14 days of ring use. Sampling at multiple time points and sites (vaginal, cervical, rectal and blood) will provide information on drug distribution, kinetics, and, by sampling after ring removal on Day 14, how long drug persists. The latter may be important as behavior studies suggest that some women may remove a ring at time of menses or around sex. To capture systemic absorption, blood will be sampled to determine drug concentrations in blood plasma and PBMCs (peripheral blood mononuclear cells). To capture the concentrations of drug within the genital tract, CVF will be sampled using Dacron swabs of the introitus, ectocervix, and area adjacent to the ring. Rectal sampling with swabs will also be obtained if participants consent to the procedure to determine drug concentrations in the rectum. Sampling at different sites (proximal and distal to the ring) will provide important information as to how well drug permeates throughout the genital tract. Cervical tissue sampling will be highly informative given that it is the likely site of drug action. However, biopsies must be taken sparingly for several reasons: they are uncomfortable to some and alter the healing process. Accordingly, two baseline biopsies will be taken prior to randomization and ring insertion to confirm absence of study drug and for PD studies. Subsequent biopsies for PK (pharmacokinetics) and PD (pharmacodynamics) studies will be delayed until the ring is removed. Following TDF IVR removal a third biopsy will be obtained for PK studies. Two cervical biopsies will be obtained following placebo IVR removal for PD studies and to blind safety data. The study will not be double-blinded because the TDF and placebo rings are not identical in appearance. Therefore, the study clinician will be able to collect two biopsies from participants in the placebo group and three biopsies from participants in the TDF ring group after ring removal. In order to maintain participant blinding, all participants will be informed that two biopsies will be taken before ring insertion and 2-3 biopsies will be taken after ring removal. Paired biopsies will provide the best data, as it will avoid inter-individual variability; both sets of cervical biopsies (pre- and post-IVR use) will be obtained during the second half of the participant's menstrual cycle (cycle days 18-23), which is prior to menses. Cervical biopsies will be obtained without local anesthetic. Participants may take acetaminophen before and/or after the biopsies are collected if desired.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- Single (Participant)
Eligibility Criteria
- Ages
- 18 Years to 45 Years (Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •General good health (by volunteer history and per investigator discretion) 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)
- •Willing to give voluntary consent, sign an informed consent form and comply with study procedures as required by the protocol
- •HIV-uninfected based on testing performed by study staff during screening procedures
- •Using low dose combined (estrogen and progesterone-containing) oral contraceptive pills (does not include extended-cycle, 24 and 28-day active pill regimens). Per participant report must be using this contraceptive method with no change in the prior 3 months and intending to use same method for the duration of study participation.
- •Currently have a regular 28-day menstrual cycle on combined oral contraceptive pills.
- •Normal Pap test at screening or appropriately documented history of Pap test and completed follow-up of any abnormal pap tests consistent with American Congress of Obstetricians and Gynecologists (ACOG) practice guidelines #99 and #
- •Agrees not to participate in other research studies involving drugs, medical devices, or vaginal products for the duration of study participation.
- •Able and willing to refrain from inserting any non-study vaginal products or objects into the vagina for the 48 hours prior to Visit 2 throughout the duration of the study.
- •Able and willing to abstain from oral, vaginal and anal sex for 48 hours prior to Visit 2 throughout the duration of the study.
Exclusion Criteria
- •Women must meet none of the following criteria prior to genital sampling at Visit 2:
- •Known adverse reaction to polyurethane or to any components of the study product or allergy to both silver nitrate and Monsel's solution.
- •Hepatitis B infection (defined as positive hepatitis B surface antigen).
- •Chronic, recurrent, and/or acute vulvar or vaginal symptoms (pain, irritation, spotting, etc.).
- •Known bleeding disorder that could lead to prolonged or continuous bleeding with biopsy.
- •Pregnant or intending to become pregnant during the period of study participation.
- •Currently breastfeeding or having breastfed an infant in the last two months, or planning to breastfeed during the course of the study.
- •Menopause.
- •History of unexplained or unresolved intermenstrual bleeding in the 3 months prior to screening.
- •History of gynecological procedures (including genital piercing) on the external genitalia, vagina or cervix in the last 14 days.
- •Hysterectomy.
- •Use and/or anticipated use during the study period of an intravaginal or intrauterine device.
- •Systemic use in the last 2 weeks or anticipated use during the study period of any of the following: corticosteroids, antibiotics, antifungals, antivirals, anticoagulants or antiretrovirals.
- •Grade 1 or higher laboratory abnormality, per the August 2009 update of the Division of AIDS, National Institute of Allergy and Infectious Disease (DAIDS) Table for Grading the Severity of Adverse Events (AEs).
- •In the last six months, diagnosed with or treated for any sexually transmitted infection (STI).
- •Reproductive tract infection (RTI) or pelvic inflammatory disease (PID) requiring treatment per current CDC (Center for Disease Control and Prevention) guidelines at Screening or Enrollment.
- •Positive test for Trichomonas vaginalis, Neisseria gonorrhea or Chlamydia trachomatis at screening.
- •Reactive test for syphilis at screening.
- •At Screening or Enrollment, has a clinically apparent Grade 1 or higher pelvic exam finding (observed by study clinician or designee) per the Division of AIDS Table for Grading the Severity of Adult and Pediatric Adverse Events, Addendum 1, Female Genital Grading Table for Use in Microbicide Studies.
Arms & Interventions
TDF Intravaginal Ring
Tenofovir Disoproxil Fumarate intravaginal ring (TDF-IVR) is a white (with clear segment), flexible torus-shaped device with an inner core compartment comprised of TDF (86 wt% of formulation) and Sodium Chloride (NaCl) (14 wt% of formulation). The intravaginal ring will be worn continuously for 14 days. It will be inserted into the vagina following cessation of participant's menses at Visit 3 and removed at Visit 7.
Intervention: TDF Intravaginal Ring (Drug)
Placebo Intravaginal Ring
The placebo intravaginal ring (IVR) is a clear, flexible torus-shaped device with an inner core which contains sodium chloride (NaCl). The intravaginal ring will be worn continuously for 14 days. It will be inserted into the vagina following cessation of participant's menses at Visit 3 and removed at Visit 7.
Intervention: Placebo Intravaginal Ring (Drug)
Outcomes
Primary Outcomes
Grade 1 Genitourinary Events or Higher as Defined by the DAIDS Table for Grading the Severity of Adult and Pediatric Adverse Events
Time Frame: 14 days of vaginal ring use
Grade 1 or higher Genitourinary events as defined by the DAIDS (Division of AIDS) Table for Grading the Severity of Adult and Pediatric Adverse Events during the trial period judged to be related to study product
Grade 2 or Higher Adverse Events as Defined by the DAIDS Table for Grading the Severity of Adult and Pediatric Adverse Events
Time Frame: 14 days of vaginal ring use
Grade 2 or higher systemic and local Adverse Events as defined by the Division of Aids (DAIDS) Table for Grading the Severity of Adult and Pediatric Adverse Events during the trial period
Secondary Outcomes
- TFV-DP C-ave in Cervical Tissue(before and after 14 days of vaginal ring use)
- TDF AUC0-14 in CVF Genital Secretions (ECX and VAG), TFV AUC0-14 in CVF Genital Secretions (ECX and VAG), and TFV AUC0-14 in Plasma(1, 3, 7 and 14 days after ring insertion and 2 and 7 days after ring removal)
- TDF and TFV Maximum Concentrations (C-max) in CVF Genital Secretions (ECX and VAG) and TFV Maximum Concentration in Plasma(1, 3, 7 and 14 days after ring insertion and 2 and 7 days after ring removal)
- TDF and TFV Time to Maximum Concentrations (T-max) in CVF Genital Secretions (ECX and VAG), and TFV Time to Maximum Concentration in Plasma(1, 3, 7 and 14 days after ring insertion and 2 and 7 days after ring removal)
- TFV C-ave in Cervical Tissue(before and after 14 days of vaginal ring use)
Investigators
Marla Keller
Prof. Dept of Medicine
Albert Einstein College of Medicine