Pulmonary Disease, Chronic Obstructive Clinical Trial
Official title:
A Randomized Cross-over Study to Evaluate the Pharmacokinetics and Pharmacodynamics of Twice Daily Oral Administration of GSK1325756, Compared to Placebo, in Healthy Subjects; and the Pharmacokinetic Profile of Twice Daily Oral Administration of GSK1325756 in Healthy Fed and Fasted Elderly Subjects
This study will invite two groups of volunteers to participate.
The data from one group of volunteers will be used to find out how much study drug, known as
GSK1325756, is in the blood after taking the drug twice in one day. Data will also collected
to find out if the level of cetain blood cells, known as neutrophils, change significantly
after taking the study drug twice in one day. This group of volunteers will be aged 40 to 64
years of age.
The data from the other group of volunteers will be used to find out if taking the study
drug, GSK1325756, twice in one day with or without food, makes a difference to the level of
study drug in the blood. This group of volunteers will also provide data to find out if any
study drug metabolites are present in the bile, a fluid secreted by the liver. This group of
volunteers will be aged 65 to 80 years of age.
The current study will be conducted in two parts. In Part A - Cohort 1, healthy fed subjects
aged 40 to 64 years (inclusive) will be enrolled to evaluate both the pharmacokinetics and
pharmacodynamics of twice daily oral administration of GSK1325756 compared to matching
placebo. In Part B - Cohort 2, healthy elderly subjects aged 65 to 80 years (inclusive) will
be enrolled to evaluate the pharmacokinetic profile of twice daily oral administration of
GSK1325756 for administered under fed and fasted conditions. Parts A and B may be performed
in parallel.
The approximate duration of the current study is expected to be between 64 and 74 days. The
study will require subjects to complete a screening visit within 30 days, followed by Part A
- Cohort 1 enrolment requiring 3 x (3 day treatment period + 7 day washout period) or Part B
Cohort 2 enrolment requiring 2 x (3 day treatment period + 7 day washout period). All
subjects will complete a follow up visit within seven to 14 days of last dose.
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