drugset / Trial / NCT01013142

Evaluate the Safety of MN-221 in Subjects With Stable Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)

NCT01013142 ↗

Phase 1 Completed 48 enrolled MediciNova
RandomizedSingle-groupQuadruple-blindTreatment

Summary

The objective of this clinical study is to determine the safety of intravenous MN-221 compared to placebo when administered in subjects diagnosed with stable moderate to severe COPD.

Timeline

Start
2009-11
Primary completion
2010-03
Completion
2010-03

Drugs

EvaluationDrugModalityDoseRoute
Subject bedoradrine Small molecule 300 ug Intravenous
Subject bedoradrine Small molecule 600 ug Intravenous
Subject bedoradrine Small molecule 1200 ug Intravenous