A Study of Ruxolitinib in Combination With Capecitabine in Subjects With Advanced or Metastatic HER2-negative Breast Cancer

PHASE2TerminatedINTERVENTIONAL
Enrollment

149

Participants

Timeline

Start Date

May 31, 2014

Primary Completion Date

February 29, 2016

Study Completion Date

January 31, 2017

Conditions
Breast Cancer
Interventions
DRUG

Ruxolitinib

"5 mg tablets to be administered by mouth~Ruxolitinib 15 mg BID (starting dose)"

DRUG

Capecitabine

Capecitabine 2000 mg/m\^2 daily given as 1000 mg/m\^2 twice a day (BID) (starting dose) Day 1-14 of each 21 day cycle

DRUG

Placebo

5 mg matching placebo tablets to be administered by mouth

Trial Locations (106)

Unknown

Birmingham

Chandler

Sedona

La Jolla

Los Angeles

Oxnard

San Diego

San Francisco

Santa Monica

Aurora

Denver

New Haven

Washington D.C.

Fort Myers

Hialeah

Miami

Plantation

St. Petersburg

Tampa

Atlanta

Marietta

Savannah

Chicago

Quincy

Springfield

Urbana

Ames

Wichita

Louisville

Baton Rouge

Baltimore

Detroit

Kalamazoo

Duluth

Minneapolis

Kansas City

St Louis

Grand Island

Omaha

Camden

Hackensack

Farmington

Albany

Johnson City

New York

The Bronx

Goldsboro

Pinehurst

Canton

Cincinnati

Cleveland

Columbus

Middletown

Portland

Bethlehem

Philadelphia

Pittsburgh

Charleston

Greenville

Chattanooga

Germantown

Nashville

Arlington

Bedford

Dallas

El Paso

Fort Worth

Houston

McAllen

Plano

Tyler

Ogden

Salt Lake City

Fairfax

Norfolk

Richmond

Salem

Seattle

Green Bay

Milwaukee

La Roche-sur-Yon

Paris

Alba

Fano

Foggia

Lecco

Milan

Naples

Pontedera

Roma

Saronno

Lisbon

A Coruña

Barcelona

Jaén

Lleida

Madrid

Cardiff

Glasgow

Kingston upon Thames

London

Nottingham

Sutton

Taunton

Truro

Yeovil

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Incyte Corporation

INDUSTRY