drugset / Trial / NCT00468689

Evaluation Of SB-751689 Administered At Supratherapeutic Dose Levels In Healthy Adult Subjects.

NCT00468689

Phase 1 Completed 15 enrolled GlaxoSmithKline
RandomizedSingle-groupSingle-blindTreatment

Summary

This study will evaluate the safety, tolerability and exposure of SB-751689 when administered alone at supratherapeutic doses and when SB-751689 is co administered with ketoconazole, a PGP/CYP3A4 inhibitor that increases exposure of SB-751689. Data from this study will enable the planning and conduct of a QTc study for SB-751689.

Timeline

Start
2007-04
Primary completion
2007-08
Completion
2007-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Ketoconazole Small molecule 200 mg Oral
Subject SB-751689 Unknown 100 ng Oral
Subject SB-751689 Unknown 400 ng Oral

Indications