drugset / Trial / NCT01294566

FTIH to Evaluate Safety, Tolerability, and Pharmacokinetics of Single Oral Doses of GSK1322888 in Healthy Caucasian and Japanese Volunteers

NCT01294566 ↗

Phase 1 Completed 17 enrolled GlaxoSmithKline
RandomizedSingle-groupSingle-blindTreatment

Summary

This study is the First Time In Human study for the motilin receptor agonist, GSK1322888. GSK1322888 is a potent and selective small molecule motilin receptor agonist, distinct from the motilide compound structures. The aims of this study are to assess the safety, tolerance, and pharmacokinetics of single oral doses of GSK1322888 and to identify a well-tolerated and safe dose that will accelerate gastric emptying of a 13C stable isotope-labeled test meal in healthy volunteers. The study will include assessment of ECGs, vital signs, safety laboratory sampling, adverse events, pharmacokinetics, and the 13C-Octanoic Acid Breath Test to measure gastric emptying.

Timeline

Start
2010-11-29
Primary completion
2011-03-23
Completion
2011-03-23

Drugs

EvaluationDrugModalityDoseRoute
Subject GSK1322888 Small molecule 1 mg Oral
Subject GSK1322888 Small molecule 2 mg Oral
Subject GSK1322888 Small molecule 5 mg Oral
Subject GSK1322888 Small molecule 10 mg Oral
Subject GSK1322888 Small molecule 20 mg Oral
Subject GSK1322888 Small molecule 25 mg Oral
Subject GSK1322888 Small molecule 40 mg Oral
Subject GSK1322888 Small molecule 80 mg Oral

Indications