Safety and Efficacy of Andecaliximab (GS-5745) in Adults With Moderately to Severely Active Ulcerative Colitis

PHASE2/PHASE3TerminatedINTERVENTIONAL
Enrollment

165

Participants

Timeline

Start Date

September 30, 2015

Primary Completion Date

September 30, 2016

Study Completion Date

November 30, 2016

Conditions
Ulcerative Colitis
Interventions
BIOLOGICAL

Andecaliximab

Andecaliximab 150 mg administered via SC injection

BIOLOGICAL

Placebo

Placebo matched to andecaliximab administered via SC injection

Trial Locations (87)

Unknown

Dothan

Wheat Ridge

Lauderdale Lakes

Miramar

Winter Park

Zephyrhills

Chicago

Topeka

Louisville

Monroe

Ann Arbor

Plymouth

St Louis

Egg Harbor

New York

Chapel Hill

Charlotte

Mentor

Rochester

Germantown

Hermitage

Arlington

Baytown

Houston

Irving

San Antonio

Southlake

Charlottesville

Chesapeake

Norfolk

Richmond

Seattle

Wauwatosa

Footscray

Herston

Malvern

Melbourne

Ghent

Leuven

Mouscron

Pleven

Victoria

Vaughan

Hradec Králové

Nantes

Békéscsaba

Budapest

Debrecen

Dublin

Rozzano

San Giovanni Rotondo

Daugavpils

Amsterdam

Christchurch

Auckland

Wellington

Bialystok

Krakow

Lublin

Piaseczno

Poznan

Sopot

Środa Wielkopolska

Tychy

Warsaw

Wroclaw

Bucharest

Timișoara

Moscow

Novosibirsk

Rostov-on-Don

Saint Petersburg

Trenčín

Claremont

Seoul

Suwon

Basel

Bern

Taichung

Kharkiv

Kyiv

Lviv

Odesa

Vinnitsa

Cambridge

Oxford

Prescot

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Gilead Sciences

INDUSTRY

NCT02520284 - Safety and Efficacy of Andecaliximab (GS-5745) in Adults With Moderately to Severely Active Ulcerative Colitis | Biotech Hunter | Biotech Hunter