Safety and Tolerability Study of Rifaximin in Participants With a History of Hepatic Encephalopathy

PHASE3CompletedINTERVENTIONAL
Enrollment

322

Participants

Timeline

Start Date

March 7, 2007

Primary Completion Date

December 8, 2010

Study Completion Date

December 8, 2010

Conditions
Hepatic Encephalopathy
Interventions
DRUG

Rifaximin

Oral

Trial Locations (35)

Unknown

Birmingham

Aurora

Fresno

La Jolla

Long Beach

Los Angeles

Merced

Sacramento

San Francisco

Golden

Washington D.C.

Macon

Iowa City

Monroe

Boston

Detroit

Kansas City

Lebanon

Bayside

New York

Rochester

Asheville

Charlotte

Cincinnati

Cleveland

Philadelphia

Houston

Odessa

San Antonio

Richmond

Madison

Calgary

Victoria

Toronto

Montreal

All Listed Sponsors
lead

Bausch Health Americas, Inc.

INDUSTRY

NCT00686920 - Safety and Tolerability Study of Rifaximin in Participants With a History of Hepatic Encephalopathy | Biotech Hunter | Biotech Hunter