drugset / Trial / NCT00679263

Study Evaluating the Safety and Effects of MN-221 in Subjects With Moderate to Severe Asthma

NCT00679263 ↗

Phase 2 Completed 17 enrolled MediciNova
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of MN-221 at two different dosing rates administered through a continuous infusion in subjects diagnosed with moderate to severe asthma.

Timeline

Start
2008-02
Primary completion
2008-07
Completion
2008-07

Drugs

EvaluationDrugModalityDoseRoute
Subject bedoradrine Small molecule 1080 ug Intravenous
Subject bedoradrine Small molecule 1125 ug Intravenous

Indications