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WithdrawnNCT00503763PSMMSSUpdated Apr 16, 2015

Efficacy and Safety of Statin on the Course of Progressive Smoldering Multiple Myeloma

A Phase 2 interventional study of Simvastatin in Smoldering Multiple Myeloma, sponsored by Meir Medical Center. Withdrawn. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2015-04-16.

Sponsored by Meir Medical Center · Phase 2, Interventional, and Treatment

Why this study was withdrawn
We found out that there is another study on the same issue
Phase
Phase 2
Study type
Interventional
Enrollment
0
Allocation
Not applicable
Ages
18 Years to 80 Years
Sex
All
01

Study summary

The aim of the study is to evaluate the effect of statin administration on the course of progressive Smoldering Multiple Myeloma.

Read the detailed description

In vitro data indicate that statins affect myeloma cells, mainly by inducing cell death and growth suppression.

This is a national, multicenter, phase IIa, single arm (not controlled), open label clinical trial of Simvastatin 80mg p.o. /day in a population of patients with progressive SMM. Patients will be treated with Simvastatin 40 mg and if no side effect will be seen the dose will be escalated to 80 mg for up to 18 months. All further treatment decisions after completion of the study are at the discretion of the investigator.Approximately 15 patients will be enrolled.

02

Conditions studied

  • Smoldering Multiple Myeloma

Keywords

  • Smoldering multiple myeloma
  • Simvastatin
  • Paraprotein
03

In context

Multiple Myeloma

3,632 studies on the registry are indexed under Multiple Myeloma; 745 are open to participants now.

Browse Multiple Myeloma studies →

Lead sponsor

Meir Medical Center is the lead sponsor of 389 studies on the registry; 34 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Patients fulfilling the criteria of SMM. (see Appendix I)
  2. Patients with progressive smoldering Myeloma. (see Appendix II)
  3. Age 18-80 years.
  4. Signed informed consent prior to patient recruitment.

Exclusion criteria

Exclusion Criteria:

  1. Patients fulfilling diagnostic criteria of active MM .(see Appendix I)
  2. Patients fulfilling diagnostic criteria of: solitary myeloma or non secreting myeloma or oligosecretory myeloma or light chain myeloma.
  3. Patients on statin treatment on the day of recruitment.
  4. Patients on chemotherapy or receiving steroids.
  5. Patients with any contraindication to statin treatment:

    • Known intolerance or hypersensitivity to statin.
    • SGOT or SGPT above 1.5 times of upper normal level (UNL).
    • CPK above UNL
    • Concomitant treatment with macrolides and or antifungal agents (ketoconazole)
    • Creatinine level above 1.5 mg%
    • Any severe and/or uncontrolled medical disease (i.e., uncontrolled diabetes, chronic renal disease, or active uncontrolled infection).
  6. Patients with second primary malignancy (except for non melanoma skin malignancy) unless they have been disease free for at least five years.
  7. Patients who have a history of alcohol or drug abuse.
  8. Patients who are mentally or physically unable to comply with all aspects of the study.
  9. Participation to an investigational drug trial
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Interventions

  • DrugSimvastatin
06

What researchers measure

Primary outcomes

  1. Paraprotein level

    Time frame: 18 months

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 16, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00503763
Lead sponsor
Meir Medical Center
Responsible party
Sponsor
First posted
Jul 19, 2007
Start date
Sep 2007
Primary completion
Mar 2009 (estimated)
Completion
Mar 2009 (estimated)
Last update
Apr 16, 2015

Study contacts

Michael Lishner, MD
principal investigator · Meir Medical Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Jul 2007. You cannot join it, but the record below documents what was studied.

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