drugset / Trial / NCT01264783

Safety and Tolerability of RNS60 Given by IV to Healthy Subjects

NCT01264783

Phase 1 Completed 12 enrolled Revalesio Corporation
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objective of this study is to evaluate the safety and tolerability of RNS60 administered intravenously to healthy subjects. 12 subjects will receive RNS60 or placebo at three escalating rates for 48 hours for each rate.

Timeline

Start
2011-07
Primary completion
2011-09
Completion
2011-09

Drugs

EvaluationDrugModalityDoseRoute
Subject RNS60 Other / unclassified Intravenous

Indications