Trials / Terminated
TerminatedNCT01772719
Overcoming Chemotherapy Resistance In Refractory Multiple Myeloma With Simvastatin and Zoledronic Acid
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 7 (actual)
- Sponsor
- University of Louisville · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to examine the effect of simvastatin and zoledronic acid on M-protein and/or free light chains when added to conventional chemotherapy for the treatment of multiple myeloma patients.
Detailed description
We hypothesize that the addition of simvastatin and zoledronic acid to bortezomib, thalidomide, melphalan or dexamethasone based regimens will decrease drug resistance when treating refractory multiple myeloma. We hypothesize that the addition of simvastatin and zoledronic acid will not increase the chemotherapy toxicity significantly and will be tolerable for patients. We believe simvastatin and zoledronic acid have antitumor properties and will contribute to reversal of resistance. Treatment will be significantly enhanced when these agents are combined
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Simvastatin and zoledronic acid | 1. Simvastatin 80 mg PO daily starting two days before starting chemotherapy and stopping two days after chemotherapy. 2. Zoledronic acid 4 mg IV over 15 minutes on day 1 and then monthly. |
Timeline
- Start date
- 2012-08-01
- Primary completion
- 2016-11-01
- Completion
- 2016-11-01
- First posted
- 2013-01-21
- Last updated
- 2019-11-18
- Results posted
- 2019-11-18
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01772719. Inclusion in this directory is not an endorsement.