drugset / Trial / NCT00919490

A Study of Single Dose of ABT-333 in Healthy Male Adults

NCT00919490 ↗

Phase 1 Completed 39 enrolled Abbott Abbott Japan Co.,Ltd · collab
RandomizedSingle-groupDouble-blindTreatment

Summary

The objectives of this study is to assess the safety, tolerability, and pharmacokinetics of blind, escalating, single, oral doses of ABT-333 under nonfasting conditions in healthy male adult in Japan.

Timeline

Start
2009-06
Primary completion
2009-08
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject dasabuvir Small molecule 400 mg Oral
Subject dasabuvir Small molecule 800 mg Oral
Subject dasabuvir Small molecule 1200 mg Oral
Subject dasabuvir Small molecule 1600 mg Oral