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:
- People who have been diagnosed with multiple myeloma that has come back or stopped responding to treatment, and who have already received at least 2 previous treatment plans, including one from a drug class called immunomodulatory drugs and one from a class called proteasome inhibitors.
- People who have previously been treated with anti-CD38 or anti-BCMA therapies (except a specific type called an anti-BCMA T cell engager), as long as their myeloma did not stop responding to anti-CD38 treatment.
- People whose myeloma can be measured through specific blood, urine, or light chain protein tests that show the disease is still active (confirm with trial site for exact thresholds).
- People aged 18 or older.
- Women who are able to become pregnant must agree to use reliable contraception during the trial and for a set period after the last dose of each study drug, and must inform their doctor immediately if pregnancy occurs or is suspected.
- People who are well enough to carry out light daily activities, as assessed by a standard health status scale (confirm with trial site).
- People whose blood counts, kidney function, and liver function meet minimum levels set by the trial (confirm with trial site for exact values).
- People who have or have had another cancer, where that cancer or its treatment is not expected to interfere with this trial's results.
- People with a history of heart disease or previous treatment with heart-affecting drugs, where a doctor's assessment places their heart function at a certain level or better on a standard heart classification scale (confirm with trial site).
- People who are able to understand the study and are willing to sign a consent form.
Who may not be able to join:
- People with active plasma cell leukemia, POEMS syndrome, or amyloidosis.
- People who have had a stem cell transplant within the past 12 weeks, or who currently have active graft-versus-host disease (a complication sometimes seen after transplants).
- People who currently have moderate or severe nerve damage in their hands or feet affecting sensation or movement.
- People who have experienced any level of nerve damage in their hands or feet from a previous anti-BCMA treatment, or who have a history of a serious nerve condition called Guillain-Barré syndrome or related conditions, or severe nerve damage affecting movement.
- People who have previously been treated with an anti-BCMA bispecific T cell engager (a specific type of targeted therapy).
- People who are currently taking part in another clinical trial using an experimental treatment.
- People who have received myeloma treatment or an experimental drug within the 2 weeks before starting this trial, or who are still experiencing side effects from a previous treatment.
- People who have a known or suspected allergy to the study drugs or any of their components, including an adhesive that contains acrylic.
- People who have had certain serious heart or blood vessel events in the past 6 months, such as a heart attack, unstable chest pain, certain heart rhythm problems, a stroke, a blood clot in the lung, or certain other related events.
- People with a known active hepatitis B, hepatitis C, or HIV infection, or any active uncontrolled bacterial, fungal, or viral infection that has not fully cleared at least 14 days before joining.
- People who have had another active cancer within the past 3 years, except for certain skin cancers or other cancers that were treated with the aim of a full cure.
- People who have had major surgery in the past 14 days, or who have a medical, psychiatric, or other condition — including recent or active thoughts of self-harm — that the investigating doctor considers would make participation unsafe or unsuitable.
- People who have received a live vaccine within 30 days before the first dose of the study treatment.
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: Noopur Raje, MD, Massachusetts General Hospital
Phone: 617-724-1969
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
Objective response rate (ORR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.