Phase 2 Myeloma Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults aged 18 or older.
- People with multiple myeloma that has come back or stopped responding to treatment, and who have already received at least 3 previous treatment regimens, including specific types of therapies (a proteasome inhibitor, an immunomodulatory drug, and an anti-CD38 antibody treatment).
- People for whom the CAR-T cell therapy called ciltacabtagene autoleucel (Carvykti) is already available.
- People who are reasonably active and able to care for themselves, as measured by a standard medical scale (ECOG score of 0, 1, or 2).
- People with a life expectancy of at least 12 weeks.
- People whose recent blood test results (taken within the past 14 days) show that their blood counts and organ function are within acceptable ranges — including red blood cells, white blood cells, platelets, liver function, and kidney function (confirm with trial site for specific numbers).
- People of childbearing potential who have had a negative pregnancy test within 7 days before joining.
- People who are sexually active and are willing to use effective contraception before, during, and for at least 30 days after the trial treatment ends.
- People willing to sign a consent form agreeing to take part.
- People willing to provide blood and bone marrow samples for research purposes.
- People willing to return to the enrolling hospital for follow-up visits during the active monitoring phase of the study.
Who may not be able to join:
- People who have an early or pre-cancerous form of the condition (such as monoclonal gammopathy of undetermined significance or smoldering multiple myeloma) or a related condition called AL amyloidosis.
- People who have not yet recovered from significant side effects of previous treatments — with an exception for mild, stable nerve-related tingling or numbness that has been stable for at least one month.
- People who are pregnant, breastfeeding, or of childbearing potential (or able to father a child) and are not willing to use adequate contraception, as the study drug is known to carry risks of harm to an unborn child.
- People who have had major surgery within 28 days before joining.
- People with serious ongoing illnesses or conditions that, in the opinion of the study doctor, would make participation unsafe or interfere with the results.
- People with a significantly weakened immune system. Note: People living with HIV who have good control of the virus and no signs of immune system weakness may still be considered eligible (confirm with trial site).
- People with certain heart or cardiovascular conditions, including uncontrolled irregular heartbeats, a heart attack or heart procedure within the past 3 months, severe heart failure, uncontrolled high blood pressure, a history of life-threatening heart rhythm problems, or an abnormal heart electrical reading above a certain level.
- People with uncontrolled ongoing infections or any other medical condition that would make participation unsafe.
- People currently taking part in another clinical trial involving a treatment for their cancer.
- People who have received a live vaccine within 6 weeks before joining.
- People who have taken certain strong medications (known as CYP3A4/5 inhibitors or inducers) — including grapefruit or St. John's Wort — within 14 days before joining. Note: short courses may be allowed with dose adjustments (confirm with trial site).
- People with a known allergy or sensitivity to the study drugs dasatinib or quercetin.
- People currently taking blood-thinning medications at full therapeutic doses (such as warfarin, heparin, or similar).
- People currently taking antiplatelet medications (such as full-dose aspirin or clopidogrel). Note: low-dose "baby" aspirin for heart protection may be allowed (confirm with trial site).
- People who have taken quinolone antibiotics (for treatment or prevention of infection) within 10 days before joining.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Yi Lin, MD, PhD, Mayo Clinic
Phone: 855-776-0015
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Minimal residual disease (MRD) negativity rate
Can't join this trial?
Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.