drugset / Trial / NCT00683449
Study Evaluating the Safety and Effects of MN-221 in Subjects Experiencing an Acute Exacerbation of Asthma
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | bedoradrine | Small molecule | 240 ug | Intravenous |
| Subject | bedoradrine | Small molecule | 450 ug | Intravenous |
| Subject | bedoradrine | Small molecule | 1080 ug | Intravenous |