Phase 2 Myeloma Trial, Recruiting NCT06158412 Sponsor: The First Affiliated Hospital of Xiamen University Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT06158412
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 18 or older
  • People who have been diagnosed with multiple myeloma, confirmed by a bone marrow test showing at least 10% abnormal plasma cells, along with measurable levels of the abnormal protein the disease produces (detectable in blood or urine tests)
  • People whose multiple myeloma has come back after treatment, or whose disease did not respond well enough to treatment (known as relapsed or refractory myeloma)
  • People whose general physical functioning is rated at a reasonable level based on a standard medical assessment scale (ECOG score of 0, 1, or 2 — confirm with trial site)
  • People who are expected to live for at least 3 more months
  • People (or their legal guardian) who are able to read, understand, and sign a consent form

Who may not be able to join:

  • People who are currently taking part in, or planning to join, another interventional clinical trial
  • People the trial doctor considers unsuitable for the study for any reason
  • People with a form of myeloma that does not produce measurable abnormal proteins (called non-secretory myeloma)
  • People who have received any myeloma treatment within approximately 2 weeks before starting the trial, or who have recently received high doses of steroid medications such as prednisone or dexamethasone
  • People who had a donor stem cell transplant within the past year and have not stopped taking immune-suppressing medications at least one month before joining
  • People with low blood counts — specifically, very low platelet or white blood cell levels
  • People with significant lung disease, including severe chronic obstructive pulmonary disease (COPD) with poor lung function test results, or moderate-to-severe asthma that has not been well controlled in the past 2 years
  • People with significant heart problems, including a heart attack within the past 6 months, uncontrolled heart failure or chest pain, certain heart rhythm problems, or an abnormal heart electrical reading above a specific threshold on an ECG
  • People with severe liver problems, unless caused by the myeloma itself
  • People whose kidneys are not filtering blood adequately (confirm specific threshold with trial site)
  • People with a known allergy to the trial treatment or to similar types of medications
  • People with serious uncontrolled medical conditions such as uncontrolled diabetes, active infections, or uncontrolled high blood pressure
  • People known to be HIV positive, or who have active hepatitis B or C infection
  • People who have had another cancer in the past 5 years, with some exceptions such as certain skin cancers or cancers considered fully cured with very low chance of return
  • People who may have difficulty following the study requirements due to conditions such as alcohol dependence, drug dependence, or psychological disorders, or where the trial doctor believes participation would not be in the person's best interest
  • People who are pregnant or breastfeeding
  • People with significant nerve damage in their hands or feet at a certain level of severity (confirm with trial site)

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 28 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

Principal Investigator: Zhijuan Lin, The First Aiffiliated hosptical of xiamen University

Phone: +8615960283462

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
The First Affiliated Hospital of Xiamen University
Registry
ClinicalTrials.gov
Start date
22 November 2023
Est. completion
31 December 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Overall response rate (ORR)

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: 28 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