Phase 2 Myeloma Trial, Recruiting NCT06759181 Sponsor: Xuzhou Medical University Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT06759181
Recruiting Phase 2

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 between 18 and 70 years old
  • People with an expected survival of more than 12 weeks
  • People who have been diagnosed with multiple myeloma through physical examination, lab tests, imaging, and tissue analysis
  • People whose multiple myeloma has not responded to treatment (refractory)
  • People whose multiple myeloma has come back after treatment (relapsed)
  • People whose liver enzyme levels (ALT and AST) are below 3 times the normal range
  • People whose bilirubin level is below 2.0 mg/dl
  • People with a quality of life/function score (KPS) above 50%, meaning they are able to carry out at least some daily activities (confirm with trial site)
  • People who do not have serious heart, liver, kidney, or other major organ disease
  • People whose myeloma returned or did not go into remission after a stem cell transplant or cellular immune therapy
  • People who are not suitable for stem cell transplantation, or for whom transplantation is not possible due to other limitations
  • People from whom blood can be collected through a vein, with no medical reasons preventing a leukapheresis procedure (a process where certain blood cells are separated and collected)
  • People who understand the trial and have voluntarily signed a written consent form

Who may not be able to join:

  • People who are pregnant, breastfeeding, or planning to become pregnant within six months
  • People with certain infectious diseases, such as HIV or active tuberculosis
  • People with an active hepatitis B or hepatitis C infection
  • People whose blood cells showed poor results during a pre-screening test — specifically, less than 10% of the targeted white blood cells were successfully modified, or the cells did not multiply sufficiently during laboratory preparation (confirm with trial site)
  • People with abnormal vital signs who are unable to cooperate with medical examinations
  • People with a mental health condition that would prevent them from cooperating with treatment or assessments
  • People with a highly allergic history or a known severe allergy, particularly to a substance called IL-2
  • People who have a widespread infection throughout the body, or a severe local infection currently requiring treatment
  • People with a serious autoimmune disease
  • People who the treating doctor considers unsuitable for the trial for other medical 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.

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
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 15162166166

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
Phase 2
Sponsor
Xuzhou Medical University
Registry
ClinicalTrials.gov
Start date
31 December 2024
Est. completion
10 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Adverse events

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