Safety Study to Evaluate MN-221 in Chronic Obstructive Pulmonary Disease (COPD) Patients

PHASE1CompletedINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

May 31, 2012

Study Completion Date

May 31, 2012

Conditions
Chronic Obstructive Pulmonary Disease
Interventions
DRUG

MN-221

This drug is intravenously infused and delivers 1200 mcg to the patient in 1 hour duration. This dose is repeated over 4 days (Day 1 1200 mcg once; Day 2 1200 mcg twice; Day 3 1200 mcg twice; Day 4 1200 mcg once).

DRUG

Placebo

This intervention consists of a placebo intravenous infusion, one that contains no active medication. During the double-blind procedure, patients will be infused with placebo intravenously one time on Day 1, twice on Days 2 and 3, and one time on Day 4.

Trial Locations (2)

78130

Central Texas Health Research, New Braunfels

78229

Sylvana Research Associates, San Antonio

Sponsors

Lead Sponsor

All Listed Sponsors
lead

MediciNova

INDUSTRY

NCT01551316 - Safety Study to Evaluate MN-221 in Chronic Obstructive Pulmonary Disease (COPD) Patients | Biotech Hunter | Biotech Hunter