Tenofovir/Levonorgestrel Intravaginal Ring and Tenofovir Intravaginal Ring

CONRAD

Status and phase: Unknown; Phase 2

Conditions: Prevention; Anti-Retroviral Agent; Contraception; HIV

Treatments: Drug: TFV/LNG IVR; Drug: Placebo IVR; Drug: TFV IVR

Study type: Interventional

Funder types: Other; Other U.S. Federal agency

Identifiers

NCT03762382

RFA-PS-17-005 (Other Grant/Funding Number)

Protocol B17-144

AID-OAA-A-14-000010 (Other Grant/Funding Number)

Details and patient eligibility

About

The purpose of the study is to evaluate the safety, pharmacokinetics and pharmacodynamics of, and the tolerability and acceptance of an intravaginal ring (IVR) delivering both tenofovir and levonorgestrel (TFV/LNG) and an IVR delivering TFV only, compared to a placebo IVR, in women in Western Kenya.

Full description

This Phase 2a clinical trial will evaluate the safety, pharmacokinetics and pharmacodynamics of, and the tolerability and adherence to two novel intravaginal rings (IVRs). The tenofovir/levonorgestrel (TFV/LNG) IVR and TFV IVRs are designed to provide HIV (and HSV-2) prevention with and without contraceptive for pregnancy prevention, respectively. Women will be protected from pregnancy by abstinence from vaginal intercourse or agreeing to consistently use condoms; concurrent use of a non-hormonal copper intrauterine device is permitted.

The study will enroll healthy, HIV-negative, non-pregnant, menstruating women aged 18-34 years, inclusive, and not currently infected with hepatitis B virus, who are assessed to be at lower risk for HIV. The goal is to enroll fifty (50) women in Western Kenya. The participants will be randomized 2:2:1 to use one of the following continuous delivery IVRs: twenty (20) women to use the TFV/LNG IVR; ten (10) women to use the TFV IVR; and ten (10) women to use the placebo IVR. Participants will attend up to ten (10) routine study visits that may include physical and pelvic exams, collection of venous blood, vaginal fluid and cervical mucus, and behavioral questionnaires. A subset of twenty (20) women will participate in in-depth interviews.

Enrollment: 50 estimated patients

Sex: Female

Ages: 18 to 34 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Female, aged 18-34 years, inclusive

• General good health (by history and per clinician 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), uterus, and cervix

• Not pregnant or planning to become pregnant

• Pre-screening HIV risk score ≤4

• Currently having regular menstrual cycles (approximately 24-35 days) OR with a history of having regular menstrual cycles before contraceptive use, by report, and resumed some menstruation or spotting (with biochemical confirmation of ovulation)

• Willing to undergo Visual Inspection with Lugol's Iodine (VILI) for cervical abnormalities during pelvic exam

• Willing to abstain from use of vaginal products other than the study product, including tampons (except for during menses) , menstrual cups, vaginally inserted cloths or other materials, spermicides, lubricants, and douches for the whole study

• Willing to abstain from any vaginal intercourse starting 48 hours before certain study visits

• Vaginal and cervical anatomy that, in the opinion of the clinician, lends itself to easy genital tract sample collection and is absent of vesicles and ulcers

• No use of hormonal contraceptives within the following periods specified for each type of contraception method:

  • Oral contraceptives (combined or progestin-only), contraceptive patch or contraceptive vaginal ring in at least two (2) months
  • Last DMPA injection received at least four (4) months ago and has resumed regular menstruation
  • Hormonal IUD/IUS removed at least four (4) months ago and has resumed regular menstruation
  • Hormonal implant removed at least six (6) months ago and has resumed regular menstruation

• Willing to refrain from using any hormonal contraceptives for the entire study and to use only study-provided non-spermicidal male condoms with or without a study-provided Cu-IUD

• P4 ≥3.0 ng/ml

• Estimated glomerular filtration rate (eGFR) ≥90ml/min/1.73m2

• Willing to give voluntary consent and sign/mark an informed consent form

• Willing and able to comply with protocol requirements

Exclusion criteria

• Body mass index (BMI) ≥30 kg/m
• History of hysterectomy
• Currently pregnant or within less than three (3) calendar months of the last pregnancy outcome.
• Currently breastfeeding or having breastfed an infant in the last two (2) months, or planning to breastfeed during the course of the study
• Contraindication to any study products-LNG, TFV, or excipient ingredients
• Contraindication to LNG
• In the last three (3) months, diagnosed with or treated for any STI or pelvic inflammatory disease
• Positive test for HIV-1, syphilis, Trichomonas vaginalis (TV), Neisseria gonorrhea (GC), Chlamydia trachomatis (CT) or HBsAg
• Nugent score greater than or equal to 7 or a symptomatic BV clinical diagnosis as defined by Amsel's criteria
• Suspected breast cancer or other progestin-sensitive cancer
• Suspected hepatic disease, including cirrhosis or viral hepatitis
• History of bleeding or coagulation problems
• Known current drug or alcohol abuse which could impact study compliance
• Grade 2 or higher laboratory abnormality, per 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
• Use of any concomitant medications
• 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
• History of gynecological procedures (including genital piercing) on the external genitalia, vagina, or cervix within the last 14 days
• Labial elongation (due to pulling practices and use of botanicals or caustic agents)
• Abnormal finding on laboratory or physical examination or a social or medical condition in the volunteer which, in the opinion of the site co-PI(s), would make participation in the study unsafe or would complicate interpretation of data
• Currently using, or has used within the preceding one (1) month, emtricitabine/tenofovir disoproxil fumarate (TDF/FTC or Truvada®) or any other tenofovir product, and/or has plans to use a non-study tenofovir product in any form during the study

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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50 participants in 3 patient groups, including a placebo group

TFV/LNG IVR (10mg/20μg) (Continuous)

Experimental group

Description:

Tenofovir/Levonorgestrel Intravaginal Ring

Treatment:

Drug: TFV/LNG IVR

TFV IVR (10mg) (Continuous)

Experimental group

Description:

Tenofovir Intravaginal Ring

Treatment:

Drug: TFV IVR

Placebo IVR (Non-eluting)

Placebo Comparator group

Description:

Placebo Intravaginal Ring

Treatment:

Drug: Placebo IVR