New study to see how well elranatamab works in everyday care for myeloma patients
NCT ID NCT07391761
First seen Jun 27, 2026 · Last updated Jul 02, 2026 · Updated 2 times
Summary
This study will observe 30 adults in Taiwan with relapsed or refractory multiple myeloma who are taking elranatamab as part of their regular care. Researchers will track how quickly the cancer responds, how long the response lasts, and overall survival. The goal is to understand the drug's real-world effectiveness and treatment patterns outside of a controlled trial.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- elranatamab
- What this could lead to
- If successful, this study could confirm that elranatamab is effective outside of clinical trials, helping doctors in Taiwan make better treatment decisions for multiple myeloma.
- What could go wrong
- This is an observational study, not a controlled trial, so results may be influenced by patient differences. It is small (30 patients) and only in Taiwan, so findings may not apply broadly.
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 1 person
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2026
- Expected to finish
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Jan 2028
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Study population will consist of RRMM patients who have initiated elranatamab in consistent with the local health authority approved product label
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: 1. Patients age ≥ 18 years at the initiation of elranatamab 2. Patients who have received at least one dose of elranatamab in consistent with the approved label in Taiwan. 3. Evidence of a personally signed and dated informed consent document (ICD) indicating that the patient (or a legally acceptable representative) has been informed of all pertinent aspects of the study. The ICD waiver is acceptable for patient who was ceased before recruitment. Exclusion criteria: Patients who participated in any prior clinical trials using elranatamab.
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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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Kaohsiung Chang Gung Memorial Hospital
Kachsiung, 833, Taiwan
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Linkou Chang Gung Memorial Hospital
Taoyuan, 333, Taiwan
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Taichung Veterans General Hospital
Taichung, 40705, Taiwan
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Taipei Veterans General Hospital
Taipei, 11217, Taiwan
More trials for these conditions
Other studies related to the condition(s) this trial covers.