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

PHASE2CompletedINTERVENTIONAL
Enrollment

17

Participants

Timeline

Start Date

February 29, 2008

Primary Completion Date

July 31, 2008

Study Completion Date

July 31, 2008

Conditions
Asthma
Interventions
DRUG

MN-221

Initial dose: 16 μg/min for 15 minutes followed by 8 μg/min for 105 minutes (2-hour infusion with a total dose of 1,080 μg)

DRUG

MN-221

Subsequent dose: 30 μg/min for 15 minutes followed by 15 μg/min for 45 minutes (1-hr infusion with a total dose of 1,125 μg).

DRUG

Placebo

Placebo intravenous infusion with dosing volume equivalent to active treatment.

Trial Locations (4)

29615

Greenville Pharmaceutical Research, Greenville

65401

Clinical Research of the Ozarks, Rolla

66219

PRA International, Lenexa

02747

Northeast Medical Research Associates, North Dartmouth

Sponsors

Lead Sponsor

All Listed Sponsors
lead

MediciNova

INDUSTRY

NCT00679263 - Study Evaluating the Safety and Effects of MN-221 in Subjects With Moderate to Severe Asthma | Biotech Hunter | Biotech Hunter