Lab tests could pick the right drug for tough myeloma cases
NCT ID NCT03389347
First seen Jun 27, 2026 · Last updated Sep 17, 2026 · Updated 2 times
Summary
This study tests a new way to choose treatments for people with multiple myeloma or plasma cell leukemia that has returned or stopped responding to standard therapy. Researchers use a lab test that checks many drugs at once, along with genetic information, to find which drug or drug combination might work best for each person. The goal is to see if this personalized approach is practical and can improve treatment choices for 40 participants.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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40 people
The number who actually took part.
- Started
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Feb 2018
- Finished
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Jul 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosis of multiple myeloma or plasma cell leukemia with documented relapsed or refractory disease according to International Myeloma Working Group (IMWG) criteria, in any one of the following categories: * 3 prior lines of therapy including an immunomodulatory drug (IMiD) and a proteasome inhibitor (PI) * Less than a very good partial response (VGPR) to initial therapy * Early relapse (\< 12 months) after autologous hematopoietic cell transplant (HCT) or after 1st line of therapy * Collection of a bone marrow, fluid or tissue sample that is expected to have enough cells to run the assay * Measurable disease defined by one of the following: * Serum monoclonal protein \>= 0.5 g/dL by serum protein electrophoresis (SPEP) * \>= 200 mg/monoclonal protein in urine on 24 hr urine protein electrophoresis (UPEP) * Involved serum free light chain (FLC) \>= 10 mg/dL and abnormal involved:uninvolved ratio * Plasma cytomas that are palpable per exam or measurable per standard radiologic review * Circulating plasma cells \>= 2,000 if diagnosis of plasma cell leukemia * Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-3 * Female patients of child bearing potential and non-vasectomized male patients agree to practice appropriate methods of birth control * Ability to understand purpose and risks of the study and provide signed and dated informed consent, and authorization to use protected health information * Expected survival is \> 100 days * Adequate organ function as determined by the investigator Exclusion Criteria: * Mucosal or internal bleeding, or platelet transfusion refractory * Any medical conditions that would impose excessive risk to the patient, or would adversely affect his/her participation in the study * Known active infection requiring antibiotics within 7 days of initiation of study treatment, unless considered controlled in the opinion of the investigator * Other malignancy with life expectancy \< 1 year due to the other malignancy * Pregnant or breast feeding women * Serious psychiatric illness, alcoholism, or drug addiction * Human immunodeficiency virus (HIV), or active hepatitis B or C infection * Previous treatments for multiple myeloma (MM) within 2 weeks of initiation of study treatment * Prior autologous or allogeneic stem cell transplantation (SCT) within 12 weeks of initiation of study treatment * Prior allogeneic hematopoietic cell transplantation (HCT) with active graft versus host disease (GVHD) on therapeutic dosing of immunosuppression or prednisone \> 20 mg daily equivalent * Prior major surgical procedure or radiation treatment within 2 weeks of initiation of study treatment (not including limited radiation used for palliation of bone pain)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Fred Hutch/University of Washington Cancer Consortium
Seattle, Washington, 98109, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Banking blood and bone marrow to decode plasma cell disorders
- Engineered donor cells could outsmart relapsed myeloma
- Can a Triple-Drug cocktail tame resistant myeloma?
- Can a One-Two drug punch beat back Hard-to-Treat myeloma?
- CAR-T breakthroughs come with infection risks – new study aims to decode them
- Real-world data on multiple myeloma immunotherapies could reshape monitoring and improve survival