drugset / Trial / NCT00937872

A Clinical Study to Evaluate the Pharmacokinetics and the Absolute Bioavailability of SRT2104 Given as a 250mg Oral Suspension and Intravenous Microdose of 100 µg Carbon-14 Radio-labeled SRT2104 in Healthy Male Subjects

NCT00937872

Phase 1 Completed 9 enrolled Sirtris, a GSK Company GlaxoSmithKline · collab
CrossoverOpen-labelBasic science

Summary

The primary objective of this study is to determine the absolute bioavailability of SRT2104 as a 250 mg suspension, and to define the intravenous pharmacokinetics of SRT2104. The secondary objective of this study is to assess the potential systemic metabolite burden of SRT2104, and to provide plasma and urine samples for subsequent metabolite profiling and identification.

Timeline

Start
2008-11-22
Primary completion
2008-12-22
Completion
2008-12-22

Drugs

EvaluationDrugModalityDoseRoute
Subject SRT2104 Small molecule 100 ug Oral
Subject SRT2104 Small molecule 250 mg Oral