TMC649128HPC1001 - First In-human Trial to Examine Safety, Tolerability, and Pharmacokinetics (How the Drug is Absorbed Into the Bloodstream) of Increasing Single Oral Doses of TMC649128 in Healthy Volunteers

Tibotec Pharmaceutical

Status and phase

Completed

Phase 1

Conditions

Healthy Volunteer

Treatments

Drug: TMC649128

Study type

Interventional

Funder types

Industry

Identifiers

NCT01288677

TMC649128HPC1001 (Other Identifier)

CR017272

Details and patient eligibility

About

The purpose of this study is to assess the pharmacokinetics, safety, and tolerability of single oral doses of TMC649128 in healthy volunteers. Pharmacokinetics (PK) means how the drug is absorbed into the bloodstream, distributed in the body, and eliminated from the body.

Full description

TMC649128 will be investigated for the treatment of chronic hepatitis C infection. This is a Phase I, first in humans (no clinical studies have been performed to date), double-blind (neither the participant nor investigator knows whether they receive active or placebo), randomized (study medication is assigned by chance), placebo-controlled study to examine the safety, tolerability, and blood and plasma pharmacokinetics of increasing single oral doses of TMC649128. The single dose escalation will consist of 6 sessions (Sessions I to IV) in 6 panels (Panels 1 to 6) of 9 healthy adult volunteers each. The dose of TMC649128 will be consecutively escalated. In each session, 6 participants will receive TMC649128 and 3 participants will receive placebo, all with standard meals. Each session will have a staggered approach, ie, the first 4 participants will be dosed, followed by at least a 72-hour safety review and if no acute effects are observed, the remaining 5 participants will be dosed. The main focus of the trial is the determination of safety and tolerability of TMC649128 after single oral doses in fed conditions in healthy volunteers, but also the determination of the pharmacokinetic characteristics (level-profile of TMC649128 over time in the blood stream and urine). This evaluation requires multiple blood samples from Day 1 to Day 4. Safety assessments (blood and urine tests, blood pressure, pulse, electrocardiogram, and physical examination) will follow a different schedule and will be performed during each session, up to 4 weeks after the last administration. Safety and tolerability evaluations will be recorded at regular intervals throughout the trial. The single dose escalation will consist of 6 sessions in 6 panels of 9 healthy adult volunteers each. The dose of TMC649128 will be consecutively escalated.

Enrollment

54 patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Healthy based on a medical evaluation including medical history, physical examination, blood tests and electrocardiogram
Body Mass Index of 18.0 to 30.0 kg/m² and non-smoker for at least 3 months prior to selection
Women must be postmenopausal for at least 2 years and/or be surgically sterile.

Exclusion criteria

Infection with Hepatitis A, B or C virus
infection with the Human Immunodeficiency Virus (HIV)
History of, or any current medical condition which could impact the safety of the participant in the study
A positive urine drug test at screening
History of any drug allergy or clinically relevant skin disease
Participation in an investigational drug trial or received an investigational vaccine within 30 days prior to intake.