Finding studies
Finding studies
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Lead
GlaxoSmithKline
This protocol describes the first administration of GSK2018682 to humans. The study will evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of single ascending doses of GSK2018682. The study will also provide preliminary evidence of the potential therapeutic dose-range by measuring the inhibitory effect of GSK2018682 on total lymphocyte counts.
Age
18–55
Sex
ALL
Healthy volunteers
Accepted
