XeNA Study - A Study of Xeloda (Capecitabine) in Patients With Invasive Breast Cancer

PHASE4CompletedINTERVENTIONAL
Enrollment

157

Participants

Timeline

Start Date

August 31, 2005

Primary Completion Date

April 30, 2009

Study Completion Date

July 31, 2009

Conditions
Breast Cancer
Interventions
DRUG

capecitabine [Xeloda]

825mg/m2 po bid on days 1-14 of each 3 week cycle

DRUG

Taxotere

75mg/m2 iv on day 1 of each 3 week cycle

DRUG

Herceptin (HER2-neu positive patients only)

4mg/kg iv (loading dose) followed by 2mg/kg iv weekly

DRUG

capecitabine [Xeloda]

825mg/m2 po bid on days 1-14 of each 3 week cycle

DRUG

Taxotere

75mg/m2 iv on day 1 of each 3 week cycle

Trial Locations (38)

10003

New York

15213

Pittsburgh

17901

Pottsville

21201

Baltimore

24211

Abingdon

29150

Sumter

29425

Charleston

29442

Georgetown

31405

Savannah

32910

Melbourne

33136

Miami

33321

Tamarac

38104

Memphis

38120

Memphis

44718

Canton

46227

Indianapolis

46260

Indianapolis

52242

Iowa City

55435

Edina

63141

St Louis

65109

Jefferson City

65401

Rolla

71301

Alexandria

75231

Dallas

87102

Albuquerque

87108

Albuquerque

87505

Santa Fe

90057

Los Angeles

90640

Montebello

92123

San Diego

92262

Palm Springs

06030

Farmington

04074

Scarborough

07754

Neptune City

87131-5636

Albuquerque

28233-3549

Charlotte

75390-9034

Dallas

05401

Burlington

All Listed Sponsors
lead

Hoffmann-La Roche

INDUSTRY

NCT00127933 - XeNA Study - A Study of Xeloda (Capecitabine) in Patients With Invasive Breast Cancer | Biotech Hunter | Biotech Hunter