Blood test may end painful bone marrow biopsies for myeloma patients
NCT ID NCT07691034
First seen Jul 08, 2026 · Last updated Jul 09, 2026 · Updated 1 time
Summary
This study tests whether a blood test using mass spectrometry can detect minimal residual disease (tiny amounts of cancer left after treatment) in multiple myeloma patients. Currently, doctors must take bone marrow samples, which is painful and inconvenient. The blood test would be easier and could be done more often. Researchers will compare the blood test results with standard bone marrow tests and PET scans in 40 patients who are in deep remission.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could replace painful bone marrow biopsies with a simple blood test for monitoring multiple myeloma remission.
- What could go wrong
- This is a small, early-stage study. The blood test may not be sensitive enough to catch all residual cancer cells, and results need validation in larger trials.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2035
An estimate. End dates often move.
- 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.
Who is studied
Multiple Myeloma patients in stringent complete remission for for than six months
- 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: * Multiple Myeloma patients in sCR for more than 6 months * Diagnostic bone marrow and blood/serum material biobanked at diagnosis according to established diagnostic biobank * Informed, written consent Exclusion Criteria: * Phychiatric disease or other condition where the subject may be non-compliant * Not able to read and understand Danish language * Bleeding disorder, thrombocyte counts below 20 mia/L
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- A phase i study to evaluate the safety and immunogenicity of 3D189 in patients with hematologic malignancies
- Daratumumab, pomalidomide and dexamethasone for Del(17p) positive relapsed and Relapsed/Refractory multiple myeloma patients [DEDALO]
- Can a platform trial match the right drug combo to each tumor?
- Can a Four-Drug cocktail tackle Hard-to-Treat myeloma spread?
- Can a protein boost immune recovery after myeloma transplant?