Impact of Weekly Administration of Rifapentine and Isoniazid on Steady State Pharmacokinetics of Tenofovir Alafenamide in Healthy Volunteers (YODA)

Sponsor

National Institutes of Health Clinical Center (CC) (NIH)

Overall Status

Recruiting

CT.gov ID

NCT03510468

Collaborator

(none)

Enrollment

Location

Arm

62.4

Anticipated Duration (Months)

1.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Background:

Human immunodeficiency virus (HIV) is treated with antiretroviral drugs. Many people with HIV also have the lung infection tuberculosis (TB). Most TB treatments are complicated. A simpler treatment of two TB drugs can be taken once a week. Researchers want to study how the HIV and TB drugs affect each other so people who take both can be treated safely.

Objective:

To study if rifapentine and isoniazid affect blood levels of the common antiretroviral TAF.

Eligibility:

Healthy adults ages 18-65 without HIV, TB, or hepatitis

Design:

Participants will fast before the screening visit. They will have a medical history, physical exam, and blood tests. Women may have a pregnancy test.

During the study, participants must:

Use effective birth control

Not take most medicine

Not drink alcohol

At the baseline visit, participants will repeat screening tests and get TAF tablets.

Participants will take TAF once a day for 31 days. They will keep track of doses and side effects.

Over 32 days, participants will have 4 long visits and 4 short.

At all visits, participants will:

Fast the night before

Get food

Take that day s TAF

Review their TAF supply

Have pregnancy and blood tests

Report side effects

At 3 visits, participants will also take the 2 TB drugs and vitamin B6.

At 3 long visits, participants will also have blood collected 8 times over 8 hours by plastic tube in an arm vein.

Around Day 46, participants will fast and have blood and pregnancy tests. Two weeks later, they will get a call to see how they are feeling....

Condition or Disease	Intervention/Treatment	Phase
Healthy Volunteers	Drug: Vemlidy (tenofivir alafenamide) Drug: Priftin (rifapentine) Drug: Isoniazid Dietary Supplement: Pyridoxine	Phase 1

Detailed Description

Rifapentine (RPT) is a long-acting rifamycin that can be used weekly with isoniazid (INH) as a first-line regimen in the treatment of latent tuberculosis infection (LTBI). Although this regimen offers several potential benefits, the use of weekly RPT plus INH is limited in adults infected with human immunodeficiency virus (HIV) on antiretroviral therapy (ART) due to lack of drug interaction data with antiretrovirals (ARVs). Tenofovir alafenamide (TAF) is a preferred backbone agent by the current Department of Health and Human Services ARV guidelines and is a part of multiple recommended first-line regimens for the treatment of HIV. However, the use of TAF with rifamycins, including RPT, is not recommended due to potential drug interactions. Thus, the purpose of this study is to determine the effects of concomitant RPT and INH administration on the steady state pharmacokinetics (PK) of plasma TAF, plasma tenofovir (TFV), and intracellular TFV diphosphate (dp).

This is an open-label, fixed sequence, intrasubject drug-drug interaction study designed to evaluate the steady state PK of TAF, TFV, and TFV-dp with coadministration of once-weekly RPT

INH administered at doses used to treat LTBI. The study will consist of two phases: (1) TAF once daily alone (days 1-14) and (2) TAF once daily + weight-based RPT + INH once weekly (days 15-31). Participants will undergo periodic serial ARV PK blood draws over 24 hours on days 14-15, 22-23, and 31-32.

TAF, TFV, and TFV-dp PK will be determined using non-compartmental methods. The following PK parameters will be compared between phases: area under the curve over the dosing interval, maximum plasma concentration, time to maximum plasma concentration, terminal half-life, apparent oral clearance, and minimum plasma concentration. Adverse events will be graded and recorded.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

75 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Basic Science

Official Title:

Impact of Weekly Administration of Rifapentine and Isoniazid on Steady State Pharmacokinetics of Tenofovir Alafenamide in Healthy Volunteers

Actual Study Start Date :

Jun 12, 2018

Anticipated Primary Completion Date :

Aug 23, 2023

Anticipated Study Completion Date :

Aug 23, 2023

Arms and Interventions

Arm	Intervention/Treatment
Experimental: 1 (1) TAF once daily alone (days 1-14) and (2) TAFonce daily + weight-based RPT + INH (withpyridoxine) once weekly (days 15-31)	Drug: Vemlidy (tenofivir alafenamide) Each tablet of Vemlidy contains 25 mg of tenofivir alafenamide. Drug: Priftin (rifapentine) Each tablet of Priftin contains 150 mg of rifapentine. Participants who weigh 45 to < 50 kg will take 750 mg (5 tablets), and participants who weigh (Bullet) 50 kg will take 900 mg (6 tablets). Drug: Isoniazid Each tablet of generic INH is formulated as 100 or 300 mg of the drug. Dietary Supplement: Pyridoxine Each tablet of pyridoxine contains 50 mg of Vitamin B6.

Arm

Intervention/Treatment

Experimental: 1

(1) TAF once daily alone (days 1-14) and (2) TAFonce daily + weight-based RPT + INH (withpyridoxine) once weekly (days 15-31)

Drug: Vemlidy (tenofivir alafenamide)

Each tablet of Vemlidy contains 25 mg of tenofivir alafenamide.

Drug: Priftin (rifapentine)

Each tablet of Priftin contains 150 mg of rifapentine. Participants who weigh 45 to < 50 kg will take 750 mg (5 tablets), and participants who weigh (Bullet) 50 kg will take 900 mg (6 tablets).

Drug: Isoniazid

Each tablet of generic INH is formulated as 100 or 300 mg of the drug.

Dietary Supplement: Pyridoxine

Each tablet of pyridoxine contains 50 mg of Vitamin B6.

Outcome Measures

Primary Outcome Measures

Plasma area under the curve during the dosing interval of 0 to 24hours (AUC0-24hr), maximum total plasma concentration (Cmax), time to maximum plasma concentration (tmax), terminal half-life (1/2), apparent oral clearance (CL/F), etc. [Days 14-15, 22-23, and 31-32 at 0 (pre dose), 0.25,0.5,1,2,4,6,8 and 24 hours post dose.]
To evaluate the effect of once-weekly administration of weight-based RPT + INH (+ pyridoxine) on the steady-state plasma PK of TAF and TFV (administered as TAF 25 mg).

Secondary Outcome Measures

(1) Intracellular AUC0-24hr and t (Omega) for TFV-dp. (2) AEs and abnormal laboratory values, as graded according to the DAIDS AE table and the Toxicity Grading Scale for Healthy Adult and Adolescent Volunteers Enrolled in Preventive Vaccine Tri... [Days 14-15, 22-23, and 31-32 at 0 (pre dose), 0.25,0.5,1,2,4,6,8 and 24 hours post dose.]
(1) To evaluate the effect of once-weekly administration of weight based RPT + INH (+ pyridoxine) on the steady-state intracellular PK of TFV diphosphate (dp). (2) To evaluate the safety of coadministration of TAF with once-weekly RPT +INH (+ pyridoxine) through documentation of adverse events (AEs) according to the Division of AIDS (DAIDS) AE Table for Grading the Severity of Adult and Pediatric Adverse Events Table and the Toxicity Grading Scale for Healthy Adult and Adolescent Volunteers Enrolled in Preventive Vaccine Trials AE table (total bilirubin [Tbili] only).

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 65 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

PARTICIPANT INCLUSION CRITERIA:

Individuals must meet all of the following criteria to be eligible for study participation:

Ages 18-65 years.
Weight greater than or equal to 45 kg and less than or equal to 120 kg OR body mass index greater than or eqaul to 18.0 and < 30.
Judged to be healthy based on medical history, physical examination, vital signs, and clinical laboratory tests: liver function tests (AST, ALT, Tbili) less than or equal to upper limit of normal [ULN], SCr less than or equal to ULN, platelets (PLT) > 150,000/microL, hemoglobin (Hgb) > 13 g/dL (males); greater than or equal to 12g/dL (females), C-reactive protein (CRP) less than or equal to ULN, CK less than or equal to 2x ULN, fasting total cholesterol < 240 mg/dL, or fasting triglycerides < 240 mg/dL, urine glucose < grade 2 (per DAIDS AE table), urine protein < grade 2 (per DAIDS AE table).
Negative QuantiFERON-TB Gold test at screening.
HIV-negative, as determined by standard serologic assays for HIV infection.
No laboratory evidence of active or chronic hepatitis A, B, or C infection.
Willing to abstain from alcohol consumption throughout the study period.
Agrees to genetic testing and storage of specimens for future research.
Able to provide informed consent.
Negative serum or urine pregnancy test for females of child-bearing potential.
Participants must agree not to become pregnant or impregnate a partner for the duration of the study. The use of hormonal contraceptives will not be permitted. Study participants must use one of the following methods of birth control when engaging in sexual activities that can result in pregnancy, beginning at screening until the final study visit.
Male or female condom.
Diaphragm or cervical cap with a spermicide.
Intrauterine device without hormones.

PARTICIPANT EXCLUSION CRITERIA:

Individuals meeting any of the following criteria will be excluded from study participation:

Known hypersensitivity to TAF, TDF, INH, RPT, and other rifamycin analogues.
History or presence of any of the following:
Latent or active TB infection.
Gastrointestinal (GI) disease that is uncontrolled, requires daily treatment with medication, or would interfere with a participant s ability to absorb drugs (eg, diarrhea, pancreatitis, or peptic ulcer disease).
Renal impairment (chronic renal insufficiency of any chronic kidney disease stage, or acute renal failure not induced by drug therapy defined as eGFR < 90 mL/min or SCr > ULN).
Respiratory disease that is uncontrolled or requires daily treatment with medication (eg, asthma or chronic obstructive pulmonary disease).
Cardiovascular disease (eg, hypertension [systolic blood pressure > 140 mm Hg or diastolic blood pressure > 90 mm Hg], heart failure, or arrhythmia).
Metabolic disorders (eg, diabetes mellitus).
Hematologic or bleeding disorders (eg, anemia, hemophilia, serious/major bleeding events, menorrhagia [female participants]).
Immunologic disorders.
Hormonal or endocrine disorders.
Psychiatric illness that would interfere with their ability to comply with study procedures or that requires daily treatment with medication.
Seizure disorder, with the exception of childhood febrile seizures.
Any current or history of malignancy, with the exception of cutaneous basal cell carcinoma,non-invasive squamous cell carcinoma, or any other malignancies not requiring systemic

therapy.

Current or history of osteopenia and osteoporosis.
Current participation in an ongoing investigational drug protocol or use of any investigational drug within 30 days (based on last dose received) prior to receipt of any study drugs.
Therapy with any prescription, over-the-counter (OTC), herbal, or holistic medications, including hormonal contraceptives by any route, within 5 half-lives of the agent prior to receipt of any study medications will not be permitted with the following exception: Intermittent or short-course therapy (<14 days) with prescription or OTC medications, herbals, or holistic medications within the screening period prior to starting study drugs may be permitted, and will be reviewed by investigators on a case-by-case basis for potential drug interactions. Receipt of influenza vaccination will be allowed prior to, during, and/or after the study.
Inability to obtain venous access for sample collection.
Inability to swallow whole capsules and/or tablets.
Pregnant or breastfeeding.
Drug use that may impair safety or adherence.
Use of nicotine-containing products, including cigarettes and chewing tobacco, nicotine patches, gum, electronic cigarettes, etc.
Organ or stem cell transplant recipient.
Uncorrected and persistent electrolyte abnormalities (eg, potassium, magnesium, and calcium).
Current alcohol use disorders (DSM-5 criteria).
Fasting total cholesterol > 240 mg/dL or fasting triglycerides > 240 mg/dL at screening.
Any condition that, in the opinion of the investigator, contraindicates participation in this study.