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Sponsored by: |
Bayside Health |
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Information provided by: | Bayside Health |
ClinicalTrials.gov Identifier: | NCT00164086 |
The purpose of this trial is to study the effects of a medication already widely used to treat cardiovascular disease and diabetes, in reducing the progression of myeloma.
Condition | Intervention | Phase |
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Myeloma |
Drug: atorvastatin |
Phase I |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study |
Ages Eligible for Study: | 18 Years to 80 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Dr Jennifer Martin, MBChB, FRACP | 0405 341 676 | jennifer.martin@med.monash.edu.au |
Australia, Victoria | |
Alfred Hospital | |
Melbourne, Victoria, Australia, 3181 |
Principal Investigator: | Andrew Spencer, MBChB, FRACP, PhD | The Alfred |
Study ID Numbers: | 7/04 |
Study First Received: | September 13, 2005 |
Last Updated: | October 10, 2006 |
ClinicalTrials.gov Identifier: | NCT00164086 History of Changes |
Health Authority: | Australia: Department of Health and Ageing Therapeutic Goods Administration |
Antimetabolites Antilipemic Agents Anticholesteremic Agents Hydroxymethylglutaryl-CoA Reductase Inhibitors |
Atorvastatin Neoplasms, Plasma Cell Multiple Myeloma |
Antimetabolites Molecular Mechanisms of Pharmacological Action Therapeutic Uses Antilipemic Agents Enzyme Inhibitors |
Anticholesteremic Agents Hydroxymethylglutaryl-CoA Reductase Inhibitors Pharmacologic Actions Atorvastatin |