A Phase 1 Study Examining the Pharmacokinetics and Tolerability of a Single Oral Dose of Bendavia (MTP-131)

Stealth BioTherapeutics Inc.30 enrolled

Overview

The purpose of this study is to assess the study medication blood levels after administration of a single oral capsule of Bendavia at one of three dose levels. The effects of Bendavia on the volunteers will also be assessed.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

BASIC_SCIENCE

Masking

TRIPLE

Enrollment

Conditions

Healthy

Interventions

Bendavia 10mgDRUG

Bendavia 50mgDRUG

Bendavia 100mgDRUG

PlaceboDRUG

Eligibility

Sex: ALLMin age: 18 YearsMax age: 65 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Healthy adult males or females aged between 18 and 65 years of age with signed informed consent. * Women who are not post-menopausal (without menstrual bleed for \>24 months) or surgically sterile must have a negative serum pregnancy test at screening and within 24 hours of treatment with understanding (through informed consent process) to not become pregnant over the duration of the study and must agree to employ an effective form of birth control for the duration of the study. * Acceptable forms of birth control are: double-barrier contraceptives (condom, diaphragm with spermicide) or intra-uterine device 1 week prior to and at least 30 days post treatment even if hormonal contraceptives are used. Exclusion Criteria: * Serum sodium level below the lower limit of the site's clinical laboratory normal range at the study qualification visit, * Clinically significant laboratory abnormalities as determined by the Principal Investigator at laboratory screening * Creatinine clearance calculated by the Cockcroft and Gault method calculated to be \<90 mL/min for males and \<80 mL/min for females * Clinically significant abnormalities on physical examination, * Body weight less than 60 or greater than 80 kg and a body mass index of less than 18 kg/m2 or greater than 32 kg/m2, * Any disease or condition that might compromise the cardiovascular, hematological, renal, hepatic, pulmonary (including chronic asthma), endocrine (e.g., diabetes), central nervous, or gastrointestinal (including an ulcer) systems, * History of seizures or history of epilepsy, * History of serious (Principal Investigator judgment) mental illness, * Participant in any research involving investigational product within 30 days before planned date of drug administration, * Positive serology for human immunodeficiency virus type 1 or 2, hepatitis B surface antigen, or hepatitis C, * Fever greater than 37.5°C at the time of planned dosing, * Suspicion, or recent history, of alcohol or substance abuse, * Donated blood or blood products within the past 30 days, * Women who are pregnant or breastfeeding, * Employee or family member of the investigational site, * Subjects who currently smoke cigarettes, cigars, pipes or chew tobacco products or who have used any tobacco product in the 30 days prior to screening, * Subjects who are either unwilling to agree to refrain from use or found to be using: * Alcohol, caffeine, xanthine-containing food or beverages, nicotine products and over-the-counter medications with the exception of Tylenol from 24 hours prior to dosing and throughout the confinement period * Prescription medications from 14 days prior to, and 7 days post, dose (excluding hormonal contraceptives) * Hormonal contraceptives without concomitant use of double-barrier contraceptives (condom, diaphragm with spermicide) for a period of 7 days prior to, and 30 days post, dose * Subjects having previous exposure to Bendavia

Locations (1)

Clinical Pharmacology of Miami

Miami, Florida, United States

Outcomes

Primary Outcomes

Mean peak plasma concentration (Cmax) of Bendavia (ng/ml) in each cohort.

Blood drawn at pre-dose (immediately prior to study drug ingestion), 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 18, 24, 36, and 48 hours post-dose will be assessed for Bendavia plasma concentrations. Mean Cmax is defined as the mean of maximum concentration reported for each subject by cohort.