Overview

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

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
Participant gender:
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.
Phase:
Phase 1
Details
Lead Sponsor:
Abbott
Collaborator:
Abbott Japan Co.,Ltd