GSK Investigational Site
Fukuoka, 812-0025, Japan
NCT Number: NCT00964405
This is a randomised, double blind, placebo-controlled, 2-parts study to investigate the safety, tolerability, and pharmacokinetics of single and repeat inhaled doses of GSK233705 from a novel dry powder device in healthy Japanese male subjects.
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Notify Me20 year–64 year
Male
Interventional
Phase 1
Fukuoka, 812-0025, Japan
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
AST(GOT), ALT(GPT), total-bilirubin: below the upper limit of the normal ranges
Exclusion criteria
Inhaled Long acting muscarinic receptor antagonist
Matching placebo
GlaxoSmithKline
Industry
Phase I Study of GSK233705- A Randomised, Double Blind, Placebo-controlled, 2-parts Study to Investigate the Safety, Tolerability, and Pharmacokinetics of Single and Repeat Inhaled Doses of GSK233705 From a Novel Dry Powder Device in Healthy Japanese Male Subjects -
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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