Study Comparing the Safety and Efficacy of Intravenous CXA-201 and Intravenous Levofloxacin in Complicated Urinary Tract Infection, Including Pyelonephritis

PHASE3CompletedINTERVENTIONAL
Enrollment

558

Participants

Timeline

Start Date

June 20, 2011

Primary Completion Date

August 11, 2013

Study Completion Date

September 4, 2013

Conditions
Complicated Urinary Tract InfectionPyelonephritis
Interventions
DRUG

CXA-201

CXA-201 IV infusion (1500mg q8) for 7 days

DRUG

Levofloxacin

Levofloxacin IV infusion (750mg qd) for 7 days

Trial Locations (76)

Unknown

San Diego

Wheat Ridge

Hialeah

Teaneck

Charleston

Belo Horizonte

Porto Alegre

Joinville

Campinas

Sao Jose de Rio Preto

Rio de Janeiro

São Paulo

Santiago de Cali

Armenia

Barranquilla

Bogotá

Kohtla-Järve

Tallinn

Tartu

Tbilisi

Giessen

Lübeck

Miskolc

Gyor

Szentes

Sopron

Salgótarján

Nyíregyháza

Zalaegerszeg

Budapest

Tatabánya

Kfar Saba

Petah Tikva

Tel Litwinsky

Haifa

Jerusalem

Safed

Daugavpils

Liepāja

Riga

Valmiera

Ventspills

Guadalajara

Chihuahua City

San Luis Potosí City

Veracruz

Chisinau

Oradea

Bucharest

Timișoara

Brasov

Bucharest

Iași

Sibiu

Kemerovo

Moscow

Nizhny Novgorod

Novosibirsk

Penza

Saint Petersburg

Saratov

Belgrade

Banská Bystrica

Levice

Martin

Prešov

Skalica

Bloemfontein

Pretoria

Soweto

Middleburg

Bellville

Nakorn Ratchasima

Chiang Mai

Lopburi

Prachuap Khiri Khan

All Listed Sponsors
lead

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

INDUSTRY

NCT01345929 - Study Comparing the Safety and Efficacy of Intravenous CXA-201 and Intravenous Levofloxacin in Complicated Urinary Tract Infection, Including Pyelonephritis | Biotech Hunter | Biotech Hunter