Study Comparing the Safety and Efficacy of Intravenous CXA-201 and Intravenous Meropenem in Complicated Intraabdominal Infections

PHASE3CompletedINTERVENTIONAL
Enrollment

494

Participants

Timeline

Start Date

December 23, 2011

Primary Completion Date

October 3, 2013

Study Completion Date

October 15, 2013

Conditions
Complicated Intra-abdominal Infection
Interventions
DRUG

CXA-201 and metronidazole

CXA-201 IV infusion (1500mg q8h) and metronidazole IV infusion (500mg q 8h) for 4-14 days

DRUG

Meropenem

Meropenem IV infusion (1000mg q8h) for 4-14 days

Trial Locations (61)

Unknown

Springfield

Boston

Robbinsdale

Columbus

Ciudadelo-Buenos Aires

General Rodríguez

La Plata

Loma Hermosa

Luján

Merlo

Tandil

Vicente López

Paraná

Corrientes

Córdoba

Santa Fe

Pleven

Sofia

Varna

Temuco

Santiago

Split

Zagreb

Kohtla-Järve

Tallinn

Tartu

Freiburg im Breisgau

Heidelberg

Gyula

Szeged

Szentes

Győr

Zalaegerszerg

Budapest

Kaposvár

Kecskemét

Vác

Kfar Saba

Tel Litwinsky

Beer Yahkov

Haifa

Liepāja

Riga

Kaunas

Klaipėda

Šiauliai

Vilnius

Chisinau

Krakow

Lubin

Wołomin

Szczecin

Lodz

Belgrade

Krafujevac

Niš

Novi Sad

Wŏnju

Incheon

Suwon

Seoul

All Listed Sponsors
lead

Cubist Pharmaceuticals LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)

INDUSTRY

NCT01445678 - Study Comparing the Safety and Efficacy of Intravenous CXA-201 and Intravenous Meropenem in Complicated Intraabdominal Infections | Biotech Hunter | Biotech Hunter