drugset / Trial / NCT00683449

Study Evaluating the Safety and Effects of MN-221 in Subjects Experiencing an Acute Exacerbation of Asthma

NCT00683449 ↗

Phase 2 Terminated 29 enrolled MediciNova
RandomizedParallel-groupSingle-blindTreatment

Summary

The objective of this clinical study is to examine the safety and effectiveness of intravenous MN-221 compared to placebo when administered as an adjunct to standard therapy in subjects experiencing an acute exacerbation of asthma.

Timeline

Start
2008-06
Primary completion
2009-03
Completion
2009-03

Outcome

Outcome not reported

Stopped: “Data from Dose Groups 1,2 and other MN-221 studies resulted in the determination of a more appropriate dosing scheme for MN-221 in subjects with asthma.”

Drugs

EvaluationDrugModalityDoseRoute
Subject bedoradrine Small molecule 240 ug Intravenous
Subject bedoradrine Small molecule 450 ug Intravenous
Subject bedoradrine Small molecule 1080 ug Intravenous

Indications