drugset / Trial / NCT01171391

VA106483 Dose Response in Females

NCT01171391 ↗

Phase 1 Completed 21 enrolled Vantia Ltd
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to describe the pharmacokinetics and pharmacodynamics of VA106483 in female subjects.

Timeline

Start
2010-07
Primary completion
2010-11
Completion
2010-11

Drugs

EvaluationDrugModalityDoseRoute
Subject VA106483 Small molecule 4 mg Intravenous

Indications

No indication recorded.