Breathlessness mystery: can a finger device predict side effects in myeloma treatment?
NCT ID NCT04827563
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to find out why some multiple myeloma patients develop shortness of breath when taking the drug carfilzomib. Researchers used an FDA-approved finger device called EndoPAT to check blood vessel health and tracked symptoms through surveys. The study enrolled 50 adults with newly diagnosed or relapsed multiple myeloma who were already receiving carfilzomib. The goal was to gather information to better prevent this side effect in the future.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- carfilzomib
- What this could lead to
- If successful, this could help doctors predict and prevent shortness of breath in multiple myeloma patients receiving carfilzomib.
- What could go wrong
- This is a small, terminated pilot study, so results may be limited. It does not test a new treatment, only gathers information.
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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50 people
The number who actually took part.
- Started
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Mar 2021
- Finished
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Sep 2025
- Lead sponsor
-
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
Participants with multiple myeloma who are being treated with carfilzomib.
- Ages
-
18 years and older
- Sex
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Anyone
- Healthy volunteers
-
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: * Age ≥ 18 * Confirmed diagnosis of multiple myeloma * Newly-diagnosed multiple myeloma, or relapsed/refractory multiple myeloma with receipt of 1-3 previous lines of therapy and with a 2-week washout from prior therapy * Receiving carfilzomib as either standard-of-care therapy or as part of a clinical trial Exclusion Criteria: * Previous receipt of anthracycline chemotherapy * Previous receipt of carfilzomib * Four or more previous lines of therapy * Active pregnancy at the time of enrollment
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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
-
University of Chicago
Chicago, Illinois, 60637, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Bispecific antibody combo aims to deepen myeloma responses
- Can a stronger drug cocktail give older myeloma patients a better start?
- Three oxygen sensors, one question: can site differences flag the sickest breathless patients?
- Cheap blood count ratios eyed as window into Myeloma's inflammatory grip
- Can a t-cell engager rescue myeloma that outsmarted CAR-T?
- Can myeloma treatment work without steroids?