Bioavailability, Food Effect and Safety, Tolerability of a New Oral Suspension in Comparison to the Marketed Moxifloxacin Tablet in Healthy Adults

PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

May 31, 2010

Primary Completion Date

November 30, 2010

Study Completion Date

January 31, 2011

Conditions
Healthy
Interventions
DRUG

Moxifloxacin (Avelox, BAY12-8039)

Single oral dose of moxifloxacin (Avelox, BAY12-8039) IR (immediate release) tablet 400 mg under fasting conditions

DRUG

Moxifloxacin (BAY12-8039)

Single oral dose of moxifloxacin (BAY12-8039) oral suspension 400 mg under fasting conditions

DRUG

Moxifloxacin (BAY12-8039)

Single oral dose of moxifloxacin (BAY12-8039) oral suspension 400 mg under fed conditions

Trial Locations (1)

42096

Wuppertal

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY