drugset / Trial / NCT01480271

An Investigation of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GSK2245035 in Healthy Volunteers and Allergic Rhinitics.

NCT01480271

Phase 1 Completed 61 enrolled GlaxoSmithKline
RandomizedSingle-groupQuadruple-blindTreatment

Summary

GSK2245035 is a highly selective Toll-like Receptor 7(TLR7) agonist capable of preferentially inducing the production of interferon alpha (IFNα) versus tumor necrosis factor alpha (TNFα). The aim of this FTIH study is to collect tolerability, pharmacokinetic (PK) and pharmacodynamic (PD) information to enable the identification of appropriate safe doses of intranasal (i.n) GSK2245035, associated with up-regulation of TLR7-mediated genes in the nasal milieu, for use in subsequent clinical drug development studies. There will be two parts to the study: Healthy Volunteers will be dosed in escalating single doses in Part 1, followed by Allergic Rhinitis (AR) subjects dosed similarly in Part 2.

Timeline

Start
2011-05-30
Primary completion
2011-09-30
Completion
2011-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject GSK2245035 Small molecule 2 ng Intranasal
Subject GSK2245035 Small molecule 20 ng Intranasal
Subject GSK2245035 Small molecule 100 ng Intranasal
Subject GSK2245035 Small molecule 200 ng Intranasal
Subject GSK2245035 Small molecule 400 ng Intranasal
Subject GSK2245035 Small molecule 1000 ng Intranasal
Subject GSK2245035 Small molecule 2000 ng Intranasal
Subject GSK2245035 Small molecule 4000 ng Intranasal