Study to Evaluate the Efficacy and Safety of Reslizumab Treatment in Patients With Moderate to Severe Asthma

PHASE3CompletedINTERVENTIONAL
Enrollment

511

Participants

Timeline

Start Date

February 29, 2012

Primary Completion Date

August 31, 2013

Study Completion Date

August 31, 2013

Conditions
Eosinophilic Asthma
Interventions
DRUG

Reslizumab

Reslizumab administered at a dosage of 3.0 mg/kg by intravenous (iv) infusion by qualified study personnel every 4 weeks for 16 weeks (for a total of 4 doses).

DRUG

Placebo

Matching placebo administered by intravenous (iv) infusion by qualified study personnel every 4 weeks for 16 weeks (for a total of 4 doses).

Trial Locations (66)

Unknown

Investigational Site 861, Birmingham

Investigational Site 842, Homewood

Investigational Site 887, Jasper

Investigational Site 809, Tucson

Investigational Site 892, Tucson

Investigational Site 846, Little Rock

Investigational Site 828, Anaheim

Investigational Site 900, Fresno

Investigational Site 862, Huntington Beach

Investigational Site 852, Los Angeles

Investigational Site 909, Los Angeles

Investigational Site 864, Newport Beach

Investigational Site 812, Rancho Mirage

Investigational Site 808, Riverside

Investigational Site 804, Sacramento

Investigational Site 837, Centennial

Investigational Site 851, Denver

Investigational Site 832, Wheat Ridge

Investigational Site 855, Jacksonville

Investigational Site 865, Miami

Investigational Site 881, Miami

Investigational Site 805, Albany

Investigational Site 870, Stockbridge

Investigational Site 816, Chicago

Investigational Site 824, Shiloh

Investigational Site 883, Evansville

Investigational Site 878, Fort Wayne

Investigational Site 820, Lenexa

Investigational Site 873, Owensboro

Investigational Site 801, Lafayette

Investigational Site 877, Mandeville

Investigational Site 875, White Marsh

Investigational Site 871, Fall River

Investigational Site 834, North Dartmouth

Investigational Site 889, Troy

Investigational Site 838, Rolla

Investigational Site 818, St Louis

Investigational Site 841, St Louis

Investigational Site 857, Albuquerque

Investigational Site 819, Newburgh

Investigational Site 844, Charlotte

Investigational Site 845, Middleburg Heights

Investigational Site 810, Tulsa

Investigational Site 859, Ashland

Investigational Site 859, Portland

Investigational Site 854, Jenkintown

Investigational Site 843, Providence

Investigational Site 802, Florence

Investigational Site 814, Orangeburg

Investigational Site 821, Spartanburg

Investigational Site 829, Spartanburg

Investigational Site 850, Knoxville

Investigational Site 803, Nashville

Investigational Site 880, Dallas

Investigational Site 858, Dickinson

Investigational Site 869, Live Oak

Investigational Site 879, Plano

Investigational Site 847, Salt Lake City

Investigational Site 876, West Jordan

Investigational Site 840, Fairfax

Investigational Site 836, Richmond

Investigational Site 867, Seattle

Investigational Site 833, Spokane

Investigational Site 904, Vancouver

Investigational Site 806, Greenfield

Investigational Site 823, La Crosse

All Listed Sponsors
lead

Teva Branded Pharmaceutical Products R&D, Inc.

INDUSTRY

NCT01508936 - Study to Evaluate the Efficacy and Safety of Reslizumab Treatment in Patients With Moderate to Severe Asthma | Biotech Hunter | Biotech Hunter