Simvastatin in Waldenstrom's Macroglobulinemia
Stopped early · Phase 2
Conditions studied: Waldenstrom's Macroglobulinemia
In brief
This research study seeks to find new ways to treat people with Waldenstrom's Macroglobulinemia (WM). The study is for participants with slow growing WM who otherwise might not need therapy for at least 3-6 months. Simvastatin is a drug approved by the FDA for lowering cholesterol. In test tube studies the study drug appears to have direct anti-cancer effect against WM tumor cells and mast cells.
Key facts
- Study ID
- NCT00575965
- Run by
- Dana-Farber Cancer Institute
- People needed
- 18
- Starts
- 2007-11-01
- Expected to finish
- 2011-12-01
- Last updated by the study team
- 2015-12-16
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 18 years of age or older
- Clinicopathological diagnosis of Waldenstrom's macroglobulinemia
- Measurable disease
- Slowly progressing disease not requiring therapy for at least 3-6 months and who do not meet consensus panel criteria for initiation of therapy
- ECOG Performance status of 0 or 1
- Adequate organ function as defined in the protocol
- Patients should agree to avoid grapefruit juice which is a major inhibitor of CYP 3A4
You may not qualify if…
- Patients who have had chemotherapy or radiotherapy within 4 weeks prior to entering the study, or those who have not recovered from adverse events due to agents administered more than four weeks earlier
- Patients who have had rituximab within 3 months prior to entering the study
- Patients who have taken any Statin in the past
- Patients who take cyclosporin, danazol, or gemfibrozil will be excluded
- Prior history of rhabdomyolysis
- Uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with the study requirements
- Pregnant or breastfeeding women
- HIV-positive
- Patients who take verapamil will be excluded
- Patients with active or history of liver disease
- Patients who consume more than three alcoholic beverages per day
Where it is running
- Dana-Farber Cancer Institute — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
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