Fluoroquinolone Resistance Prevalence Study
Stopped early
Conditions studied: Multiple Myeloma
In brief
This is an exploratory study to determine the prevalence of fluoroquinolone resistance in patients receiving dose-intense melphalan with autologous peripheral blood stem cell (PBSC) transplantation in the treatment of multiple myeloma (MM). These data may be used in subsequent studies exploring the use of prophylaxis in this patient population.
Key facts
- Study ID
- NCT05824689
- Run by
- Hackensack Meridian Health
- People needed
- 124
- Starts
- 2022-07-08
- Expected to finish
- 2025-01-15
- Last updated by the study team
- 2026-06-05
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects >18 yrs of age.
- Diagnosis of multiple myeloma undergoing (first or subsequent) autologous PBSC transplantation.
- Transplant conditioning with melphalan 200 mg/m2.
- PBSC cell dose of >2x10e6 CD34+ cells/kg.
- Able to receive fluoroquinolone prophylaxis.
- Subjects must give consent for enrollment into this study.
You may not qualify if…
- Unwillingness to provide informed consent.
- Enrollment into a treatment protocol prescribing antibiotic prophylaxis.
- A diagnosis other than multiple myeloma.
- Receiving a conditioning regimen other than melphalan 200 mg/m2.
- Known light-chain amyloid deposition in any organ.
Where it is running
- Lombardi Comprehensive Cancer Center, Georgetown University — Washington D.C., District of Columbia, United States
- John Theurer Cancer Center, Hackensack Meridian Health — Hackensack, New Jersey, United States
Full record on ClinicalTrials.gov
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