A Study of Maribavir Pediatric Formulation in Healthy Adult Participants

NCT ID: NCT05918822

Last Updated: 2024-09-26

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 32 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-07-25
• Study Completion Date: 2023-09-01

Brief Summary

The study will have 2 parts, Part 1 and Part 2. Participants will only participate in one part.

The main aim of Part 1 of this study is to check the ability of a single dose of maribavir pediatric formulation to be absorbed in the digestive tract compared to commercial tablet formulation and to check how a high-fat, high-calorie meal affects absorption, distribution, and elimination of maribavir pediatric formulation given orally as water suspension.

The main aim of Part 2 of this study is to assess the stomach acid reducing effect of multiple doses of rabeprazole on absorption, distribution, and elimination of maribavir pediatric formulation given orally as water suspension.

Each participant will stay in the study clinic from the day before the first treatment until the day after the last treatment.

Detailed Description

Part 1 is a crossover design with three treatments (Treatments A, B, and C), six sequences, and three periods.

The relative bioavailability of 200 milligrams (mg) maribavir pediatric formulation administered orally as water suspension under fasting conditions (Treatment B) will be compared to 200 mg maribavir commercial tablet administered orally under fasting conditions (Treatment A). In addition, the effect of food on the pharmacokinetics (PK) of 200 mg maribavir pediatric formulation administered orally as water suspension under fasting conditions (Treatment B) and fed conditions (Treatment C) will be assessed. In each sequence, participants will receive three treatments (Treatments A, B, and C) per schedule.

• Sequence 1: Treatment A + Treatment B + Treatment C
• Sequence 2: Treatment A + Treatment C + Treatment B
• Sequence 3: Treatment B + Treatment A + Treatment C
• Sequence 4: Treatment B + Treatment C + Treatment A
• Sequence 5: Treatment C + Treatment A + Treatment B
• Sequence 6: Treatment C + Treatment B + Treatment A

Part 2 is a single fixed-sequence design with two treatments (Treatments D and E). The two treatments will be administered to evaluate the gastric acid-reducing effect of multiple doses of rabeprazole on the PK of a single dose of 200 mg maribavir pediatric formulation administered orally as water suspension.

Conditions

Healthy Volunteers

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Part 1, Sequence 1: Treatment A + Treatment B + Treatment C

Participants will receive maribavir single 200 mg commercial tablet, on Day 1 of Treatment Period 1 under fasting condition (Treatment A), followed by maribavir 200 mg pediatric powder-for-oral suspension, single oral dose on Day 1 of Treatment Period 2 under fasting condition (Treatment B), and further followed by maribavir 200 mg pediatric powder-for-oral suspension, single oral dose on Day 1 of Treatment Period 3 administered with a high fat/high calorie meal (Treatment C). There will be a washout period of a minimum of 72 hours between each treatment.

Group Type: EXPERIMENTAL

Maribavir Commercial Tablet Formulation

Intervention Type: DRUG

Maribavir commercial tablet.

Maribavir Pediatric Powder-for-oral Suspension Formulation

Intervention Type: DRUG

Maribavir pediatric powder-for-oral suspension.

Part 1, Sequence 2: Treatment A + Treatment C + Treatment B

Participants will receive maribavir single 200 mg commercial tablet, on Day 1 of Treatment Period 1 under fasting condition (Treatment A), followed by maribavir 200 mg pediatric powder-for-oral suspension, single oral dose on Day 1 of Treatment Period 2 administered with a high fat/high calorie meal (Treatment C), and further followed by maribavir 200 mg pediatric powder-for-oral suspension, single oral dose on Day 1 of Treatment Period 3 under fasting condition (Treatment B). There will be a washout period of a minimum of 72 hours between each treatment.

Group Type: EXPERIMENTAL

Maribavir Commercial Tablet Formulation

Intervention Type: DRUG

Maribavir commercial tablet.

Maribavir Pediatric Powder-for-oral Suspension Formulation

Intervention Type: DRUG

Maribavir pediatric powder-for-oral suspension.

Part 1, Sequence 3: Treatment B + Treatment A + Treatment C

Participants will receive maribavir 200 mg pediatric powder-for-oral suspension, single oral dose on Day 1 of Treatment Period 1 under fasting condition (Treatment B), followed by maribavir single 200 mg commercial tablet, on Day 1 of Treatment Period 2 under fasting condition (Treatment A), and further followed by maribavir 200 mg pediatric powder-for-oral suspension, single oral dose on Day 1 of Treatment Period 3 administered with a high fat/high calorie meal (Treatment C). There will be a washout period of a minimum of 72 hours between each treatment.

Group Type: EXPERIMENTAL

Maribavir Commercial Tablet Formulation

Intervention Type: DRUG

Maribavir commercial tablet.

Maribavir Pediatric Powder-for-oral Suspension Formulation

Intervention Type: DRUG

Maribavir pediatric powder-for-oral suspension.

Part 1, Sequence 4: Treatment B + Treatment C + Treatment A

Participants will receive maribavir 200 mg pediatric powder-for-oral suspension, single oral dose on Day 1 of Treatment Period 1 under fasting condition (Treatment B), followed by maribavir 200 mg pediatric powder-for-oral suspension, single oral dose on Day 1 of Treatment Period 2 administered with a high fat/high calorie meal (Treatment C), and further followed by maribavir single 200 mg commercial tablet, on Day 1 of Treatment Period 3 under fasting condition (Treatment A). There will be a washout period of a minimum of 72 hours between each treatment.

Group Type: EXPERIMENTAL

Maribavir Commercial Tablet Formulation

Intervention Type: DRUG

Maribavir commercial tablet.

Maribavir Pediatric Powder-for-oral Suspension Formulation

Intervention Type: DRUG

Maribavir pediatric powder-for-oral suspension.

Part 1, Sequence 5: Treatment C + Treatment A + Treatment B

Participants will receive maribavir 200 mg pediatric powder-for-oral suspension, single oral dose on Day 1 of Treatment Period 1 administered with a high fat/high calorie meal (Treatment C), followed by maribavir single 200 mg commercial tablet, on Day 1 of Treatment Period 2 under fasting condition (Treatment A), and further followed by maribavir 200 mg pediatric powder-for-oral suspension, single oral dose on Day 1 of Treatment Period 3 under fasting condition (Treatment B). There will be a washout period of a minimum of 72 hours between each treatment.

Group Type: EXPERIMENTAL

Maribavir Commercial Tablet Formulation

Intervention Type: DRUG

Maribavir commercial tablet.

Maribavir Pediatric Powder-for-oral Suspension Formulation

Intervention Type: DRUG

Maribavir pediatric powder-for-oral suspension.

Part 1, Sequence 6: Treatment C + Treatment B+ Treatment A

Participants will receive maribavir 200 mg pediatric powder-for-oral suspension, single oral dose on Day 1 of Treatment Period 1 administered with a high fat/high calorie meal (Treatment C), followed by maribavir 200 mg pediatric powder-for-oral suspension, single oral dose on Day 1 of Treatment Period 2 under fasting condition (Treatment B), and further followed by maribavir single 200 mg commercial tablet, on Day 1 of Treatment Period 3 under fasting condition as (Treatment A). There will be a washout period of a minimum of 72 hours between each treatment.

Group Type: EXPERIMENTAL

Maribavir Commercial Tablet Formulation

Intervention Type: DRUG

Maribavir commercial tablet.

Maribavir Pediatric Powder-for-oral Suspension Formulation

Intervention Type: DRUG

Maribavir pediatric powder-for-oral suspension.

Part 2: Treatment D: maribavir 200 mg

Participants will receive maribavir 200 mg pediatric powder-for-oral suspension, single oral dose on Day 1 of Treatment Period 1 under fasting condition (Treatment D).

Group Type: EXPERIMENTAL

Maribavir Pediatric Powder-for-oral Suspension Formulation

Intervention Type: DRUG

Maribavir pediatric powder-for-oral suspension.

Part 2, Treatment E: rabeprazole 20 mg + maribavir 200 mg

Participants will receive rabeprazole single 20 mg tablet, once daily on Days 1 to 5 of Treatment Period 2 under fasting condition followed by maribavir 200 mg pediatric powder-for-oral suspension, single oral dose, 2 hours after rabeprazole dosing on morning of Day 5 of Treatment Period 2 under fasting condition (Treatment E). There will be a washout period of a minimum of 72 hours between maribavir dosing in Treatment Period 1 and first dose of rabeprazole in Treatment Period 2.

Group Type: EXPERIMENTAL

Maribavir Pediatric Powder-for-oral Suspension Formulation

Intervention Type: DRUG

Maribavir pediatric powder-for-oral suspension.

Rabeprazole

Intervention Type: DRUG

Rabeprazole tablet.

Interventions

Maribavir Commercial Tablet Formulation

Maribavir commercial tablet.

Intervention Type: DRUG

Maribavir Pediatric Powder-for-oral Suspension Formulation

Maribavir pediatric powder-for-oral suspension.

Intervention Type: DRUG

Rabeprazole

Rabeprazole tablet.

Intervention Type: DRUG

Other Intervention Names

TAK-620; TAK-620

Eligibility Criteria

Inclusion Criteria

• An understanding, ability, and willingness to fully comply with study procedures and restrictions and to voluntarily sign (personally or via a legally authorized representative) informed consent form to participate in the study.
• Age 18 to 55 years, inclusive at the time of consent, at the screening visit.
• Male, or non-pregnant, non-breastfeeding female who agrees to comply with any applicable contraceptive requirements of the protocol or female of non-childbearing potential.
• Body mass index (BMI) between 18.0 and 30.0 kilogram per meter square (kg/m^2), inclusive with a body weight greater than (>) 50 kilograms (kg) (110 pounds [lbs]), at the screening visit.
• Healthy as determined by the Investigator or designee on the basis of screening evaluations and medical history.
• Hemoglobin for males greater than or equal to (>=) 135.0 gram per liter (g/L) and females >=120.0 g/L, at the screening visit and on Day -1 of Treatment Period 1.
• Ability to swallow a dose of maribavir or rabeprazole.

Exclusion Criteria

• History or presence of gastritis, gastrointestinal (GI) tract disorder, hepatic disorder or cholecystectomy, history of treated or untreated Helicobacter pylori, ulcer disease or other clinical condition which, in the opinion of the investigator or designee, may affect the absorption, distribution, metabolism, or elimination of the study drugs.
• History of any hematological, hepatic, respiratory, cardiovascular, renal, neurological or psychiatric disease, gall bladder removal, or current recurrent disease that could affect the action, absorption, or disposition of the study drugs, or clinical or laboratory assessments.
• Current or relevant history of physical or psychiatric illness, any medical disorder that may require treatment or make the participant unlikely to fully complete the study, or any condition that presents undue risk from the study drugs or procedures.
• Known or suspected intolerance or hypersensitivity to maribavir or rabeprazole (Part 2 only), closely related compounds, or any of the stated ingredients and excipients.
• Significant illness, as judged by the Investigator or designee, within 2 weeks of the first dose of the investigational drug (ID).
• Has diarrhea within 4 hours of the first dose of the ID.
• Donation of blood or blood products (example, plasma or platelets) within 60 days prior to receiving the first dose of the ID.
• Within 30 days prior to the first dose of the ID:

• Have used any investigational product (if elimination half-life is less than [<] 6 days, otherwise 5 half-lives).
• Have been enrolled in a clinical study (including vaccine studies) that, in the Investigator or designee's opinion, may impact this Takeda-sponsored study.
• Have had any substantial changes in eating habits, as assessed by the Investigator or designee.
• Systolic blood pressure >140 millimeters of mercury (mmHg) or <90 mmHg, and/or diastolic blood pressure >90 mmHg or <50 mmHg, at the screening visit.
• Corrected QT interval (QTc) >450 millisecond (msec) at the screening visit. If QTc exceeds 450 msec, the ECG should be repeated two more times and the average of the three QTc values should be used to determine the participant's eligibility.
• Known history of alcohol or other substance abuse within the last year.
• Male participants who consume more than 21 units of alcohol per week or three units per day. Female participants who consume more than 14 units of alcohol per week or two units per day (one alcohol unit = one beer or one wine [5 ounces [oz]/150 milliliter [mL]] or one liquor [1.5 oz/40 mL] or 0.75 oz alcohol).
• A positive screen for alcohol or drugs of abuse at the screening visit or on Day -1 of Treatment Period 1. Urine samples are to be tested for amphetamines, barbiturates, benzodiazepines, cannabinoids, cocaine, methadone, opiates, and phencyclidine.
• A positive Human immunodeficiency virus (HIV), Hepatitis B surface antigen (HBsAg), or Hepatitis C virus (HCV) antibody screen at the screening visit.
• Use of tobacco in any form (example, smoking or chewing) or other nicotine-containing products in any form (example, gum, patch). Ex-users must self-report that they have stopped using tobacco for at least 3 months prior to receiving the first dose.
• Routine consumption of more than two units of caffeine per day or participants who experience caffeine withdrawal headaches (One caffeine unit is contained in the following items: one 6-oz [180 mL] cup of coffee, two 12-oz [360 mL] cans of cola, one 12-oz cup of tea, three 1-oz [85 grams [g]] chocolate bars). Decaffeinated coffee, tea, or cola are not considered to contain caffeine.
• Current use of any prescription medication with the exception of hormonal contraceptives and hormonal replacement therapy. Current use of any over-the-counter (OTC) medication (including OTC multi-vitamin, herbal, or homeopathic preparations) within 14 days of the first dose. Hormonal contraceptives and hormonal replacement therapy may be permitted if the female participant has been on the same stable dose for at least 3 months prior to first dose.
• Current use of antacids, proton pump inhibitors (PPIs), or histamine type 2 (H2) antagonists within 14 days of the first dose, except for on-study rabeprazole.
• Inability or unwillingness to consume 100 percent of the high-fat, high-calorie meal (including participants with lactose or gluten intolerance).
• Female participants with a positive pregnancy test at the screening visit or on Day -1 of Treatment Period 1 or who are lactating.
• Participants on a diet incompatible with the on-study diet, in the opinion of the Investigator or designee, within the 30 days prior to the first dosing and throughout the study.
• Recent history (within 1 month) of oral/nasal cavity infections, history of gastroesophageal reflux, asthma treatment with albuterol, or zinc supplementation.
• Participants with dry mouth syndrome or burning mouth syndrome or participants suffering from dysgeusia.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Takeda

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Study Director

Role: STUDY_DIRECTOR

Takeda

Locations

Celerion

Tempe, Arizona, United States

Countries

United States

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Related Links

https://clinicaltrials.takeda.com/study-detail/837e7f476b7a4922??page=1&idFilter=TAK-620-1024

To obtain more information on the study, click here/on this link

Other Identifiers

TAK-620-1024

Identifier Type: -

Identifier Source: org_study_id