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 of any gender
- People who have a confirmed diagnosis of multiple myeloma that has come back or stopped responding to treatment, and who have already received at least 3 previous treatment regimens (including at least one type from each of two specific drug classes: a proteasome inhibitor and an immunomodulatory agent)
- People whose myeloma got worse during or within 12 months after their most recent treatment, or whose myeloma got worse within the last 6 months and did not respond to the most recent treatment
- People who the treating doctor considers unable to tolerate standard treatments may also be considered
- People whose myeloma can be measured at the time of screening through specific protein levels in the blood or urine, or through certain blood markers for a particular type of myeloma
- People whose myeloma cells test positive for certain proteins called CD19 and/or BCMA (confirmed by laboratory testing of tumour tissue; previous test results may be accepted in some cases, but a new biopsy may be needed if prior treatment targeted these proteins)
- People whose side effects from previous treatments have mostly settled, with any remaining side effects being mild (Grade 1 or lower), apart from certain blood-related effects or minor issues like hair loss
- People who are reasonably well and able to carry out daily activities, as measured by a standard medical scale (ECOG score of 0, 1, or 2)
Who may not be able to join:
- People whose life expectancy is estimated to be less than 3 months
- People who have, or have had, another active cancer — though some exceptions may apply, such as certain treated skin cancers, cervical changes that have been fully treated with no recurrence for at least 3 years, locally treated prostate cancer, or certain fully surgically treated breast conditions (confirm with trial site)
- People who have had a stem cell transplant using donor cells at any time, or their own cells within the past 3 months before the planned trial treatment
- People whose myeloma is present only as a single soft tissue growth outside the bone marrow
- People diagnosed with certain related blood or plasma cell conditions, including plasma cell leukaemia, Waldenström's macroglobulinaemia, POEMS syndrome, or primary AL amyloidosis
- People who have cancer that has spread to the brain or spinal fluid, or who have symptoms suggesting this
- People who have recently received other anti-cancer treatments and whose body has not yet cleared those treatments (within 5 half-lives of that treatment before the planned trial treatment date)
- People who have an active infection that is not under control
- People who test positive for HIV, syphilis, or certain hepatitis B or C markers with detectable virus levels in the blood — though exceptions may apply if the treating doctor considers the infection preventable or controllable with medication
- People with a known active autoimmune disease that requires ongoing treatment affecting the whole body
- People with a known serious allergic reaction to the study drug or any of its ingredients
- People who are pregnant or breastfeeding
- People who have received a live vaccine within 6 weeks before enrolling in the trial
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
Phone: +86-010-55499341
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
Dose limited toxicity (DLT); Incidence and severity of AEs and serious adverse events (SAEs); Incidence and severity of adverse events of special interest (AESI)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.