Myelogenous Leukemia, Chronic Clinical Trial
Official title:
Phase II Study of SCH66336, A Farnesyltransferase Inhibitor in Chronic Myelogenous Leukemia (CML)
NCT number | NCT00038597 |
Other study ID # | DM01-072 |
Secondary ID | |
Status | Completed |
Phase | Phase 2 |
First received | |
Last updated | |
Start date | April 30, 2001 |
Est. completion date | May 7, 2004 |
Verified date | October 2018 |
Source | M.D. Anderson Cancer Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this research is to see if giving the drug SCH66336 by mouth can improve the disease in patients with chronic or accelerated phase CML. The safety of this treatment will also be studied.
Status | Completed |
Enrollment | 13 |
Est. completion date | May 7, 2004 |
Est. primary completion date | May 7, 2004 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 16 Years and older |
Eligibility |
- Diagnosis of Philadelphia chromosome (Ph) -positive CML in chronic or accelerated
phase; - Failure to respond to or intolerance to imatinib mesylate (Gleevec); - Age >/= 16 years; - Life expectancy of >/= 2 months; - Performance status 2 or better (Zubrod); - Adequate renal and hepatic functions (creatinine and bilirubin </= 2 mg/dl); - Adequate cardiac function; - Not candidates for or have refused allogeneic transplantation; - Patients should not be receiving azoles (ketoconazole, itraconazole, fluconazole), macrolides, HIV protease inhibitors, cyclosporin or anti-seizure drugs (phenobarbital, phenytoin, carbamazepine), rifampin or isoniazid. |
Country | Name | City | State |
---|---|---|---|
United States | MDAnderson Cancer Center | Houston | Texas |
Lead Sponsor | Collaborator |
---|---|
M.D. Anderson Cancer Center |
United States,
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