Phase 1 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 aged 18 to 75 years old, of any gender
- People who have already been through at least 3 previous treatment plans for their cancer, including treatments from two specific drug groups: proteasome inhibitors and immunomodulatory agents
- People whose multiple myeloma or plasma cell leukaemia has come back, gotten worse, or stopped responding to treatment
- People whose cancer cells show a specific protein marker called GPRC5D, confirmed by a lab test on tissue such as a bone marrow sample
- People whose disease can be measured through at least one of the following: a bone marrow sample showing enough abnormal cells, a blood or urine protein test above certain levels, or a specific light chain blood test result — or, for disease outside the bone marrow, a detectable lesion of at least 2 cm in size
- People with a general health and activity level rated 0, 1, or 2 on a standard medical scale (meaning able to carry out some or all daily activities, with or without limitations) (confirm with trial site)
- People with a life expectancy of at least 12 weeks
- People whose blood counts, liver, kidneys, clotting, oxygen levels, and heart function all meet specific minimum levels set by the trial
- People (and their partners) who agree to use effective contraception from the time of consent until one year after the treatment infusion
- People who are able to sign the consent form in person before any screening begins
Who may not be able to join:
- People who have a condition called graft-versus-host disease (GVHD), or who need long-term medication to suppress their immune system
- People who have received certain cancer treatments too recently before the blood collection procedure — including some antibody therapies, chemotherapy, or other anti-cancer drugs within specific timeframes set by the trial
- People who have taken higher-dose steroid tablets (above a set threshold) within 7 days before screening, unless used for breathing or applied to the skin
- People with high blood pressure that cannot be controlled with medication
- People with serious heart conditions, including unstable chest pain, a heart attack within the past 6 months, significant heart failure, or severe irregular heartbeat
- People with unstable ongoing illnesses affecting the liver, kidneys, or metabolism that require medical management
- People who have had a different cancer in the past 5 years, with some exceptions for certain successfully treated cancers (such as specific skin cancers, early-stage cervical cancer, localised prostate cancer, or early breast cancer after surgery)
- People who have previously had an organ transplant
- People who have had major surgery within 2 weeks before the blood collection procedure, or who are planning surgery during or shortly after the study treatment
- People who have taken part in another interventional clinical trial within 1 month before signing the consent form
- People with an active uncontrolled infection requiring treatment by tablet or injection within 7 days before the blood collection procedure (with some minor exceptions)
- People who test positive for hepatitis B, hepatitis C, HIV, cytomegalovirus (CMV), or syphilis under specific testing conditions
- People who are pregnant or breastfeeding
- People with a mental health condition, a disorder affecting consciousness, or a disease of the brain or nervous system
- People whom the research team considers unsuitable for other reasons
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: Chunrui Li, Tongji Hospital
Phone: 86-13647233185
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
Incidence of dose-limiting toxicity (DLT) by dose group; Type and incidence of adverse events (AEs) and serious adverse events (SAEs) by dose group
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.