drugset / Trial / NCT00532467

Multiple Dose Safety Study of SRX251 Capsules in Healthy Volunteers

NCT00532467 ↗

Phase 1 Completed 50 enrolled Azevan Pharmaceuticals
RandomizedSingle-groupQuadruple-blindTreatment

Summary

This study is the second study to evaluate SRX251 in healthy volunteers and it represents the first multiple dose study. The primary objective of this study is to evaluate the safety and tolerability of escalating multiple oral doses of SRX251 capsules for 5 days in healthy adult volunteers. Levels of the drug in blood plasma will also be determined.

Timeline

Start
2007-09
Primary completion
2008-02
Completion
2008-02

Drugs

EvaluationDrugModalityDoseRoute
Subject SRX251 Unknown — Oral

Indications

No indication recorded.