An Extension Study to Determine the Efficacy and Safety of STI571 in Participants With Chronic Myeloid Leukemia Who Are Refractory to or Intolerant of Interferon-Alpha

PHASE2CompletedINTERVENTIONAL
Enrollment

532

Participants

Timeline

Start Date

December 6, 1999

Primary Completion Date

November 29, 2013

Study Completion Date

November 29, 2013

Conditions
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Interventions
DRUG

STI571

STI571 oral capsules or tablets.

Trial Locations (28)

10021

New York Presbyterian Hospital, New York

21231

Johns Hopkins Oncology Center, Baltimore

33612

H. Lee Moffet Cancer Center & Research Institute/Univ of South Florida, Tampa

48109

University of Michigan, Ann Arbor

48201

Wayne State University/Kamanos Cancer Center, Detroit

60611

Northwestern Univ meical School/Robert H. Lurie Comprehensive Cancer Center, Chicago

63110

C/O V. Ward - Washington Univ. school of Medicine, St Louis

77030

MD Anderson Cancer Center, University of Texas, Houston

90095

UCLA Medical Center, Los Angeles

97239

Oregon Health & sciences University, Portland

02115

Dana Faber Cancer Institute, Boston

Unknown

Novartis Investigative Site, Lille

Novartis Investigative Site, Pessac

Novartis Investigative Site, Poitiers

Novartis Investigative Site, Frankfurt

Novartis Investigative Site, Leipzig

Novartis Investigative Site, Mainz

Novartis Investigative Site, Mannheim

Novartis Investigative Site, Bologna

Novartis Investigative Site, Milan

Novartis Investigative Site, Monza

Novartis Investigative Site, Orbassano

Novartis Investigative Site, Pavia

Novartis Investigative Site, Rome

Novartis Investigative Site, Udine

Novartis Investigative Site, Basel

Novartis Investigative Site, London

Novartis Investigative Site, Newcastle upon Tyne

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY