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Clinical Trial DRUG CSTI571A2406

Title
An Open Label, Multi-Center Imatinib Roll-Over Protocol for Patients who Have Completed a Previous Novartis sponsored Imatinib Study and are Judged by the Investigator to Benefit from Continued Imatinib Treatment
Principal Investigator
Olga Frankfurt
Details
  • Status: Accepting New Patients
  • Study Type: Therapeutic, Treatment
  • Protocol No:.DRUG CSTI571A2406
Purpose
The purpose of this study is to allow continued use of imatinib (the study drug) for treatment of Gastrointestinal Stromal Tumor (GIST) or chronic myeloid leukemia (CML) and to collect long term safety data.
Overview
Imatinib is designed to stop an enzyme (protein) that causes certain cancer cells to grow and is used for the treatment of GIST and certain types of CML. Participants in this study have been a part of an earlier study and benefited from treatment with imatinib.
Eligibility
Some of the eligibility criteria include:
  • Participants are currently enrolled in a Novartis sponsored study receiving imatinib and are compliant (have followed all the rules of the other study).
Note: This is only a partial list of eligibility criteria. Please contact the Lurie Cancer Center for complete screening information if you are interested in this clinical trial.
Description of Treatment
Participants will start with the same dose of imatinib that they received in the previous study. Imatinib is a capsule that is taken by mouth. The study doctor may change a participant's dose depending on how they respond. Participants will remain on imatinib until the study ends or until the study doctor decides it is in their best interest to stop.
Contact
Sara Duffey
Clinical Research and Education Specialist
Robert H. Lurie Comprehensive Cancer Center
312.695.1102
cancertrials@northwestern.edu

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last updated: 23-Oct-14 05:08 AM

 

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