INDV-2000 First in Human

Indivior Inc.73 enrolled

Overview

This study is a single ascending dose (SAD) study conducted to identify the maximum tolerated dose (MTD) of INDV-2000. After completion of the SAD portion of the study and acceptable safety evaluation, a food-interaction, single-dose study under fed and fasted conditions will be conducted.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

TRIPLE

Enrollment

Conditions

Opioid Dependence

Interventions

INDV-2000DRUG

INDV-2000 will be administered as either powder in solution or powder in capsule, depending on dose administered.

PlaceboDRUG

Placebo will be administered as either powder in solution or powder in capsule, depending on dose administered.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 55 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Must be able to verbalize understanding the consent form, able to provide written informed consent, and verbalize willingness to complete study procedures, and be able to comply with protocol requirements, rules and regulations of the study site, and be likely to complete all the study interventions. * Must be considered a healthy male or non-childbearing female for Part I * For Part II, must be a healthy male who did not participate in Part I and willing to consume a high-fat meal. * Body mass index (BMI) within 18.0 to 30.0 kg/m\^2, inclusive (minimum weight of at least 50.0 kg at Screening) * Male subjects who are sexually active with female partners of child-bearing potential must use, with their partner, a condom plus an approved method of effective contraception from time of screening until 90 days after last dose of Investigational Medicinal Product (IMP). Additionally, male subjects must agree to not donate sperm during the study and for at least 90 days from last dose of IMP. Exclusion Criteria: * Have a medical history of clinically significant neurological, cardiovascular, renal, hepatic, chronic respiratory or gastrointestinal disease, or psychiatric disorder as judged by an Investigator, * Have clinically significant abnormal biochemistry, hematology or urinalysis results as judged by an Investigator, * Have a history of narcolepsy or other significant sleep disorders * Have disorders that may interfere with drug absorption, distribution, metabolism and excretion (ADME) processes, * Positive test results for human immunodeficiency virus (HIV)-1/HIV-2 antibodies, hepatitis B surface antigen (HBsAg) or hepatitis C antibody (HCVAb). * Serious cardiac illness or other medical condition including, but not limited to: Uncontrolled arrhythmias; History of congestive heart failure (CHF); myocardial infarction \< 6 months from receipt of first dose of IMP; uncontrolled symptomatic angina; corrected QT value (QTcF) \> 450 msec for males and \> 470 msec for females or history of prolonged QT syndrome; Have a blood pressure reading outside of the following range: systolic \< 86 or \> 149 mmHg; diastolic \< 50 or \> 94 mmHg * Current active hepatic or biliary disease. Subjects with cholecystectomy \< 90 days prior to screening. * Regular alcohol consumption in males \> 21 units per week and females \> 14 units per week (1 unit = ½ pint beer, 25 mL of 40% spirit or a 125 mL glass of wine). * Positive test result for alcohol and/or drugs of abuse at screening or prior to the first IMP administration. * Current smokers and those who have smoked within the last 90 days. Current users of e-cigarettes and nicotine replacement products, and those who have used these products within the last 90 days. * Concurrent treatment or treatment with an investigational drug within 30 days prior to the first dose. * Blood donation of approximately 500 mL within 56 days or plasma donation within 7 days of screening. * Subjects who are taking, or have taken, any prescribed or over-the-counter drugs (other than 2 g per day acetaminophen, hormone replacement therapy, hormonal contraception) or herbal remedies in the 14 days before IMP administration. Exceptions may apply on a case by case basis if considered not to interfere with the objectives of the study, as agreed by an Investigator and Sponsor's Medical Monitor. * Any consumption of food or drink containing poppy seeds, grapefruit or Seville oranges within 7 days prior to the IMP administration * Treatment with any known drugs that are moderate or strong inhibitors/inducers of cytochrome P450 (CYP) 3A4 within 30 days prior to first dose of IMP. * Known allergy or hypersensitivity to IMP or its excipients. * Any condition that, in the opinion of an Investigator, would interfere with evaluation of the IMP or interpretation of subject safety or study results. * Affiliated with, or a family member of, site staff directly involved in the study, or anyone with a financial interest in the outcome of the study. * Subjects who are unable, in the opinion of an Investigator, to comply fully with the study requirements.

Locations (1)

Altasciences Clinical Kansas

Overland Park, Kansas, United States

Outcomes

Primary Outcomes

Number of Participants With Treatment-emergent Adverse Events (TEAEs)

An adverse event (AE) was considered related to study drug if it could not reasonably be explained by other factors. A serious AE is any event that met any of the following criteria: * Death * Life-threatening * In-patient hospitalization or prolongation of existing hospitalization * Persistent or significant disability/incapacity * Congenital anomaly/birth defect * Other important medical event that may have jeopardized the participant or required an intervention to prevent an above outcome. A severe AE describes the intensity of an AE, defined as causing marked limitation in activity; medical intervention or therapy or hospitalization required. For vital sign and laboratory abnormalities assessed as AEs, intensity was graded in accordance with the Food and Drug Administration Guidance for Industry: Toxicity Grading Scale for Healthy Adult and Adolescent Volunteers Enrolled in Preventive Vaccine Clinical Trials, where Grade 3 = serious and Grade 4 = potentially life-threatening.

Time frame: From first dose of study drug to end of study participation for each cohort; 11 days in Part 1 and 7 days in Part II, Period 1 (fasted conditions) and 10 days in Part II, Period 2 (fed conditions).

Secondary Outcomes

Number of Participants With Clinically Significant Laboratory Findings

The investigator assessed abnormal laboratory values to determine clinical significance.

Time frame: From first dose of study drug to end of study participation for each cohort; 11 days in Part I and 7 days in Part II, Period 1 (fasted conditions) and 10 days in Part II, Period 2 (fed conditions).

Number of Participants With Clinically Significant Changes in Vital Signs

The investigator assessed changes in vital signs (including including blood pressure, respiratory rate, heart rate and temperature) to determine clinical significance.

Data from ClinicalTrials.gov

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Number of Participants With Clinically Significant Electrocardiogram (ECG) Findings

The investigator assessed abnormal ECG values to determine clinical significance.

Number of Participants With Clinically Significant Physical Examination Findings

Any clinically significant abnormalities observed during physical examination, including changes from baseline, were recorded as adverse events on the adverse event (AE) case report form (CRF) and are reported in the adverse events section of results below. However, these events were not recorded as physical examination findings. Therefore, clinically significant physical examination findings can not be reported separately.

Part I: Maximum Observed Plasma Concentration (Cmax) of INDV-2000 After a Single Dose

Concentrations of INDV-2000 were measured using a validated high-performance liquid chromatography with electrospray tandem Mass spectrometry (LC-MS/MS) method. Pharmacokinetic parameters based on the actual sample collection times were derived using standard non-compartmental methods.