Myeloma Trial, Recruiting NCT06515262 Sponsor: 920th Hospital of Joint Logistics Support Force of People's Liberation Army of China Condition: Myeloma
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Myeloma Trial, Recruiting

NCT06515262
Recruiting Not Applicable

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:

  • You understand the study and are willing to sign a consent form, attend follow-up visits, and complete all required steps
  • You are between 18 and 75 years old (any gender)
  • You have been officially diagnosed with Multiple Myeloma (MM) according to international standards
  • Your myeloma can be detected through specific blood or urine tests showing certain protein levels (confirm with trial site for exact measurements)
  • You have already been treated with three or more lines of therapy, including at least one of each of three specific types of drugs: a proteasome inhibitor, an immunomodulatory drug, and an anti-CD38 antibody
  • Your myeloma has come back or stopped responding to treatment
  • Your last treatment did not work, or your disease got worse within 60 days of finishing it
  • You have recovered from most side effects of your previous treatments
  • You are reasonably active in daily life and are expected to live at least 3 more months (confirm with trial site)
  • Your liver, kidneys, heart, and lungs are functioning well enough to meet specific test results (confirm with trial site for exact values)
  • A suitable vein can be accessed for a blood collection procedure

Who may not be able to join:

  • You have been diagnosed with or treated for another type of cancer (other than multiple myeloma)
  • You received certain types of cancer treatments within the past 14 days or within a recent short timeframe before blood is collected for this treatment
  • There is any sign or confirmed evidence that myeloma has spread to your brain or spinal fluid, or you have another active brain condition
  • You have been diagnosed with certain related blood or protein disorders, such as Waldenström's macroglobulinemia, POEMS syndrome, or AL amyloidosis
  • You have tested positive for hepatitis B, hepatitis C, HIV, or have detectable levels of certain viruses (such as CMV or EBV) in your blood
  • You have a history of severe allergic reactions
  • You have an unstable heart condition, have had a stroke or mini-stroke, or a heart attack within the past 6 months, or have significant heart failure
  • You have serious liver, kidney, or metabolic disease that requires ongoing medication
  • You have had graft-versus-host disease (a complication from a previous transplant) recently or are taking medication to suppress your immune system for this within the past 6 months
  • You have an active autoimmune or inflammatory disease affecting your nervous system
  • You have a cancer-related emergency that needs immediate treatment
  • You have an infection that is not under control and requires antibiotic treatment
  • You received certain medicines to stimulate blood cell growth within 1–2 weeks before the blood collection procedure
  • You used steroids or immune-suppressing medicines within 2 weeks before the blood collection procedure
  • You had major surgery within 4 weeks before the start of the treatment phase, have not fully recovered, or plan to have major surgery during the study
  • You received a live vaccine within 4 weeks before the screening visit
  • You have a serious mental illness
  • You have a history of heavy alcohol use or drug abuse
  • You are pregnant or breastfeeding, or you or your partner plan to have a baby within two years after receiving this treatment
  • The trial doctor feels for any other reason that taking part would not be right for you

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Sanbin Wang, 920th Hospital of Joint Logistics Support Force of People's Liberation Army of China

Phone: 13187424131

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

Status
Recruiting
Phase
Not Applicable
Sponsor
920th Hospital of Joint Logistics Support Force of People's Liberation Army of China
Registry
ClinicalTrials.gov
Start date
1 July 2024
Est. completion
1 November 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence of adverse events(AE) after infusion

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov