The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.
Brief Title: Tipifarnib in Treating Patients With Advanced Hematologic Cancer
Official Title: A Dose Finding Study of R115777 (NSC 702818) in Patients With Advanced Hematologic Malignancies
Study ID: NCT00005967
Brief Summary: Randomized phase I trial to study the effectiveness of tipifarnib in treating patients who have advanced hematologic cancer. Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die.
Detailed Description: OBJECTIVES: I. Determine the relationship between tipifarnib dose and inhibition of farnesylation in malignant cells of patients with advanced hematologic malignancies. II. Determine the safety profile of this drug in this patient population. III. Determine the clinical activity of this drug in these patients. OUTLINE: This is a randomized study. Patients are randomized to 1 of 4 dose levels. Patients receive oral tipifarnib twice daily for 21 days. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity. After 1 course of therapy, patients may receive subsequent therapy at the maximum tolerated dose at the investigator's discretion.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
University of Chicago Cancer Research Center, Chicago, Illinois, United States
Name: Todd M. Zimmerman, MD
Affiliation: University of Chicago
Role: STUDY_CHAIR