ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Safety and Efficacy of Imatinib Versus Interferon-α Plus Cytarabine in Patients With Newly Diagnosed Philadelphia Chromosome Positive Chronic Myelogenous Leukemia

ClinicalTrials.gov ID: NCT00333840

Public ClinicalTrials.gov record NCT00333840. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 4, 2026, 12:16 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III Study of STI571 Versus Interferon-α (IFN-α) Combined With Cytarabine (Ara-C) in Patients With Newly Diagnosed Previously Untreated Philadelphia Chromosome Positive (Ph+) Chronic Myelogenous Leukemia in Chronic Phase (CML-CP)

Study identification

NCT ID
NCT00333840
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
1,106 participants

Conditions and interventions

Interventions

  • cytarabine (ARA-C) Drug
  • imatinib mesilate Drug
  • interferon-alpha (INF-a) Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 31, 2000
Primary completion
Feb 29, 2012
Completion
Feb 29, 2012
Last update posted
Oct 13, 2013

2000 – 2012

United States locations

U.S. sites
62
U.S. states
34
U.S. cities
53
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35294
Novartis Investigative Site Montgomery Alabama 36106
Novartis Investigative Site Tucson Arizona 85724
Novartis Investigative Site Berkeley California 94704
Novartis Investigative Site Campbell California 95008
Novartis Investigative Site Duarte California 91010
Novartis Investigative Site La Jolla California 92093-0960
Novartis Investigative Site Denver Colorado 80218
Novartis Investigative Site Miami Florida 33176-2197
Novartis Investigative Site Orlando Florida 32804
Novartis Investigative Site Atlanta Georgia 30342
Novartis Investigative Site Honolulu Hawaii 96813
Novartis Investigative Site Chicago Illinois 60611
Novartis Investigative Site Chicago Illinois 60612
Novartis Investigative Site Chicago Illinois 60637
Novartis Investigative Site Decatur Illinois 62526
Novartis Investigative Site Beech Grove Indiana 46107
Novartis Investigative Site Witchita Kansas 67214
Novartis Investigative Site Louisville Kentucky 40202
Novartis Investigative Site New Orleans Louisiana 70112
Novartis Investigative Site Baltimore Maryland 21201
Novartis Investigative Site Boston Massachusetts 02115
Novartis Investigative Site Worcester Massachusetts 01665
Novartis Investigative Site Ann Arbor Michigan 48109
Novartis Investigative Site Detroit Michigan 48202-2689
Novartis Investigative Site East Lansing Michigan 48910
Novartis Investigative Site Minneapolis Minnesota 55455
Novartis Investigative Site St Louis Missouri 63110
Novartis Investigative Site Billings Montana 59101
Novartis Investigative Site Omaha Nebraska 68198-7681
Novartis Investigative Site Hackensack New Jersey 07601
Novartis Investigative Site Albuquerque New Mexico 87109
Novartis Investigative Site Albuquerque New Mexico 87131
Novartis Investigative Site Farmington New Mexico 87131
Novartis Investigative Site Buffalo New York 14263
Novartis Investigative Site New York New York 10017
Novartis Investigative Site New York New York 10021
Novartis Investigative Site New York New York 10029
Novartis Investigative Site Syracuse New York 13210
Novartis Investigative Site Chapel Hill North Carolina 27599
Novartis Investigative Site Charlotte North Carolina 28203
Novartis Investigative Site Durham North Carolina 27710
Novartis Investigative Site Winston-Salem North Carolina 27157
Novartis Investigative Site Cleveland Ohio 44195
Novartis Investigative Site Columbus Ohio 43210
Novartis Investigative Site Columbus Ohio 43215
Novartis Investigative Site Dayton Ohio 45429
Novartis Investigative Site Tulsa Oklahoma 74136
Novartis Investigative Site Portland Oregon 97239
Novartis Investigative Site Pittsburgh Pennsylvania 15224
Novartis Investigative Site Pittsburgh Pennsylvania 15232
Novartis Investigative Site Providence Rhode Island 02903
Novartis Investigative Site Spartanburg South Carolina 29303
Novartis Investigative Site Memphis Tennessee 38119
Novartis Investigative Site Nashville Tennessee 37203
Novartis Investigative Site Nashville Tennessee 37205
Novartis Investigative Site Dallas Texas 75235-9179
Novartis Investigative Site Dallas Texas 75246
Novartis Investigative Site Houston Texas 77030
Novartis Investigative Site Salt Lake City Utah 84112
Novartis Investigative Site Seattle Washington 98109-1024
Novartis Investigative Site Milwaukee Wisconsin 53215

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 101 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00333840, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 13, 2013 · Synced May 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00333840 live on ClinicalTrials.gov.

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