MMRF Molecular Profiling Protocol
Status unconfirmed
Conditions studied: Multiple Myeloma, Plasma Malignancy
In brief
This protocol is now being used as screening for the MyDRUG study
Key facts
- Study ID
- NCT02884102
- Run by
- Multiple Myeloma Research Foundation
- People needed
- 1000
- Starts
- 2015-06-01
- Expected to finish
- 2026-06-01
- Last updated by the study team
- 2025-05-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients must have a diagnosis of multiple myeloma or related malignancy
- Patients are undergoing standard of care bone marrow aspirates
- Patients (male or female) from any race or ethnicity must be at least 18 years of age at the time of registration.
- Procedure-specific signed informed consent form prior to initiation of any study-related procedures.
You may not qualify if…
- It is the enrolling study physician's discretion to decide if a patient is not fit enough to undergo a bone marrow aspirate.
- Patients who are incarcerated are not eligible to participate.
- Women who are pregnant
- Patients who have had another malignancy within the last five (5) years (except for basal or squamous cell carcinoma, or in situ cancer of the cervix) where there is a possibility to contaminate the bone marrow aspirate.
Where it is running
- Mayo Clinic - Scottsdale — Scottsdale, Arizona, United States
- City of Hope — Duarte, California, United States
- UCSF Medical Center — San Francisco, California, United States
- Mayo Clinic - Jacksonville — Jacksonville, Florida, United States
- Emory University — Atlanta, Georgia, United States
- University of Chicago — Chicago, Illinois, United States
- Massachusetts General Hospital — Boston, Massachusetts, United States
- Dana-Farber Cancer Institute — Boston, Massachusetts, United States
- University of Michigan — Ann Arbor, Michigan, United States
- Barbara Ann Karmanos Cancer Institute — Detroit, Michigan, United States
- Mayo Clinic - Rochester — Rochester, Minnesota, United States
- Washington University — St Louis, Missouri, United States
- Hackensack University Medical Center — Hackensack, New Jersey, United States
- Mount Sinai Medical Center — New York, New York, United States
- Levine Cancer Institute — Charlotte, North Carolina, United States
- Ohio State University — Columbus, Ohio, United States
- Sarah Cannon Research Institute — Nashville, Tennessee, United States
- Baylor Research Institute — Dallas, Texas, United States
- Virginia Cancer Specialists — Fairfax, Virginia, United States
- Princess Margaret Cancer Centre — Toronto, Ontario, Canada
Full record on ClinicalTrials.gov
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