Myeloma Trial, Recruiting NCT07497165 Sponsor: Shanxi Bethune Hospital Condition: Myeloma
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Myeloma Trial, Recruiting

NCT07497165
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:

  • Adults between 18 and 75 years old who have been diagnosed with Multiple Myeloma that has come back or stopped responding to treatment, confirmed using standard diagnostic guidelines
  • People who have already received at least one previous treatment course for their condition
  • People whose general physical functioning falls within an acceptable range on a standard medical scale (scored 0 to 3 out of 5, where lower numbers indicate better functioning)
  • People who are able to understand information about their treatment and follow the required check-up schedule throughout the study
  • People who have signed a written consent form agreeing to take part

Who may not be able to join:

  • People with serious problems affecting the heart, lungs, liver, or kidneys, based on specific test results falling outside set limits (confirm with trial site for exact thresholds)
  • People who still have significant side effects from previous chemotherapy that have not returned to mild levels or to how they were before treatment
  • People experiencing moderate or severe nerve damage (such as numbness, tingling, or pain in the hands or feet) from previous treatment
  • People who have had major surgery, radiation therapy, a serious infection requiring antibiotics, or another severe infection within the 14 days before joining the trial
  • People with a high-risk form of the disease where cancer plasma cells make up 20% or more of blood cells
  • People with psychiatric conditions, cognitive difficulties, or other conditions that may affect their ability to follow the study requirements
  • Women who are pregnant or breastfeeding, or people who are able to have children but are unwilling to use reliable contraception during the study
  • Male participants who are unwilling to use effective contraception or avoid sperm donation during treatment and for 3 months after the final dose
  • People who have been diagnosed with or treated for another cancer within the 2 years before joining
  • People with a known allergy or sensitivity to any of the medications used in this trial, including Epunamin, Dexamethasone, Cisplatin, Etoposide, or Cyclophosphamide
  • People who are HIV positive
  • People who have taken part in another clinical trial within 30 days before joining, or who are currently in another trial
  • People whom the trial doctor considers unsuitable for any other reason

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 20 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

Phone: +156-13485304136

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
Shanxi Bethune Hospital
Registry
ClinicalTrials.gov
Start date
1 November 2025
Est. completion
30 November 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Objective response rate (ORR) is defined as the proportion of evaluable patients who achieve complete response (CR) or partial response (PR) after treatment.

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: 20 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