Infections, Bacterial, Respiratory Tract Infection
Conditions
Keywords
tolerability,, pharmacokinetics,, first time in human,, food effect, safety,
Brief summary
Studies for GSK580416 have been completed in rats and dogs. The main toxic effects seen in animals affected the digestive system and blood cells. Study OPS106400 will be the first administration of GSK580416 in humans. Parts A and B of this study will examine the safety, tolerability, and pharmacokinetics of increasing single doses of GSK580416 with reference to placebo. Part C of the study will assess the effect of food on the safety, tolerability, and pharmacokinetics of a single dose of GSK580416 in healthy subjects.
Interventions
DRUGGSK580416
Sponsors
GlaxoSmithKline
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE
Eligibility
Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
* Healthy as determined by a physician * Healthy male or female of non-child bearing potential between 18 and 55 years of age (inclusive) * Body weight \> = 50 kg and BMI between 19 and 30 kg/m2 (inclusive)
Exclusion criteria
* Positive HIV antibody, Hepatitis B surface antigen or Hepatitis C antibody with 3 months of screening * Male and female subjects not willing to follow study specified contraceptive methods * Subjects taking any recreational drugs * Regular use of tobacco- or nicotine-containing products within 6 months prior to screening * Has participated in a clinical trial and have not received a drug within 30 days before the dose of study drug * Has exposed to more than 4 new chemical entities within 12 months before the first dosing day * Use of prescription or over-the-counter medications within 7 days or 5 half-lives (whichever is longer) prior to the first dose of study drug * Use of St. John's Wort within 28 days before the first dose of study drug * Subjects not willing to follow study specified life style restrictions * Blood donation in excess of 500 mL within a 56 days period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety assessments (adverse event, ECG and vital sign) will be performed during the study. Blood samples to determine drug levels in the body will be collected during the study. | during the study |
Secondary
| Measure | Time frame |
|---|---|
| Blood samples to determine drug levels in the body will be collected during the study. | during the study |
Countries
Australia
Outcome results
None listed