Myeloma Trial, Recruiting NCT05618041 Sponsor: Hebei Senlang Biotechnology Inc., Ltd. Condition: Myeloma
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Myeloma Trial, Recruiting

NCT05618041
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:

  • People who are willing and able to follow all study requirements, including visits, treatments, and lab tests, and who have signed a consent form agreeing to take part
  • People who have been diagnosed with lymphoma, leukemia, or myeloma that has come back or has not responded to previous treatment
  • People whose cancer cells carry the specific targets that CAR-T cell therapy is designed to work against, confirmed by laboratory testing
  • People aged 14 to 75 years (inclusive), any gender
  • People whose general physical functioning is rated at a level showing they are able to carry out light activity (an ECOG performance score of 2 or below)
  • People whose haemoglobin level is at least 70g/L (blood transfusions to reach this level are allowed)
  • People whose liver, kidney, heart, and lung function meet specific minimum standards set by the trial (confirm exact values with the trial site)
  • People with a T-cell type tumour who meet specific requirements about how the tumour cells appear in the blood, based on laboratory testing (confirm details with trial site)
  • People with plans to become pregnant who agree to use contraception during the study and for six months after, and who agree to immediately inform the research team if pregnancy occurs or is suspected
  • People, or their legal guardian, who understand and have signed the informed consent form
  • People whose life expectancy is longer than three months

Who may not be able to join:

  • People with severe heart failure
  • People with a history of severe lung disease
  • People who also have another advanced cancer diagnosis
  • People with a severe or ongoing infection that cannot be brought under control
  • People with a serious autoimmune disease or a condition where the immune system does not work properly from birth
  • People with active hepatitis B or hepatitis C, confirmed by blood testing
  • People with HIV infection or syphilis
  • People with a history of severe allergic reactions to biological products, including antibiotics
  • People who have had a stem cell transplant from a donor within the last six months
  • People who have previously received CAR-T therapy or any other gene-modified cell therapy
  • People where the trial doctor believes participation could increase health risks or affect the reliability of the study results

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 15 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: Weiwei w Tian, MD, Shanxi Bethune Hospital

Phone: 008613485304136

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
Hebei Senlang Biotechnology Inc., Ltd.
Registry
ClinicalTrials.gov
Start date
7 September 2022
Est. completion
6 September 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Safety: Incidence and severity of adverse events; Efficacy: Remission Rate

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: 15 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