Dexamethasone or Dexamethasone in Combination With Thalidomide as Salvage Therapy
Completed · Phase 2
Conditions studied: Multiple Myeloma
In brief
The purpose of this investigational trial is to find out how well patients respond and how long their response lasts when treated with a standard regimen of dexamethasone with or without thalidomide and also find out what kind of side effects patients will experience.
Key facts
- Study ID
- NCT00083902
- Run by
- University of Arkansas
- People needed
- 190
- Starts
- 1998-06-01
- Expected to finish
- 2005-05-01
- Last updated by the study team
- 2010-07-02
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- All patients must have a confirmed diagnosis of previously treated, active multiple myeloma, with hypoproliferative/low risk relapse following at least one autologous transplant.
- Patients must be 18 years of age or older. Women of childbearing age and fertile men must use a medically acceptable means of birth control while on study and for 6 months thereafter.
- Patients must sign an informed consent to participate in this study, and be fully aware of the known teratogenic potential of this drug combination.
- Patients must have a SWOG performance status of 0-2.
- Patients must have adequate renal function, as defined by serum creatinine < or = 3.0 mg/dl.
- Patients must be off chemotherapy (including steroids) and local radiotherapy for > or equal 3 weeks prior to entering the study.
You may not qualify if…
- No other concurrent therapy for myeloma is permitted while on protocol.
- There must be no evidence of active infection requiring IV antibiotics.
Where it is running
- University of Arkansas for Medical Sciences/MIRT — Little Rock, Arkansas, United States
Full record on ClinicalTrials.gov
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