Phase 1 Myeloma Trial, Recruiting NCT05219721 Sponsor: Chunrui Li Condition: Myeloma
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Phase 1 Myeloma Trial, Recruiting

NCT05219721
Recruiting Phase 1

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 to 75 years old, of any gender
  • People who have already been through at least 3 previous treatment plans for their cancer, including treatments from two specific drug groups: proteasome inhibitors and immunomodulatory agents
  • People whose multiple myeloma or plasma cell leukaemia has come back, gotten worse, or stopped responding to treatment
  • People whose cancer cells show a specific protein marker called GPRC5D, confirmed by a lab test on tissue such as a bone marrow sample
  • People whose disease can be measured through at least one of the following: a bone marrow sample showing enough abnormal cells, a blood or urine protein test above certain levels, or a specific light chain blood test result — or, for disease outside the bone marrow, a detectable lesion of at least 2 cm in size
  • People with a general health and activity level rated 0, 1, or 2 on a standard medical scale (meaning able to carry out some or all daily activities, with or without limitations) (confirm with trial site)
  • People with a life expectancy of at least 12 weeks
  • People whose blood counts, liver, kidneys, clotting, oxygen levels, and heart function all meet specific minimum levels set by the trial
  • People (and their partners) who agree to use effective contraception from the time of consent until one year after the treatment infusion
  • People who are able to sign the consent form in person before any screening begins

Who may not be able to join:

  • People who have a condition called graft-versus-host disease (GVHD), or who need long-term medication to suppress their immune system
  • People who have received certain cancer treatments too recently before the blood collection procedure — including some antibody therapies, chemotherapy, or other anti-cancer drugs within specific timeframes set by the trial
  • People who have taken higher-dose steroid tablets (above a set threshold) within 7 days before screening, unless used for breathing or applied to the skin
  • People with high blood pressure that cannot be controlled with medication
  • People with serious heart conditions, including unstable chest pain, a heart attack within the past 6 months, significant heart failure, or severe irregular heartbeat
  • People with unstable ongoing illnesses affecting the liver, kidneys, or metabolism that require medical management
  • People who have had a different cancer in the past 5 years, with some exceptions for certain successfully treated cancers (such as specific skin cancers, early-stage cervical cancer, localised prostate cancer, or early breast cancer after surgery)
  • People who have previously had an organ transplant
  • People who have had major surgery within 2 weeks before the blood collection procedure, or who are planning surgery during or shortly after the study treatment
  • People who have taken part in another interventional clinical trial within 1 month before signing the consent form
  • People with an active uncontrolled infection requiring treatment by tablet or injection within 7 days before the blood collection procedure (with some minor exceptions)
  • People who test positive for hepatitis B, hepatitis C, HIV, cytomegalovirus (CMV), or syphilis under specific testing conditions
  • People who are pregnant or breastfeeding
  • People with a mental health condition, a disorder affecting consciousness, or a disease of the brain or nervous system
  • People whom the research team considers unsuitable for other 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 1: approximately ~10% 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: Chunrui Li, Tongji Hospital

Phone: 86-13647233185

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 1
Sponsor
Chunrui Li
Registry
ClinicalTrials.gov
Start date
17 March 2022
Est. completion
1 September 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence of dose-limiting toxicity (DLT) by dose group; Type and incidence of adverse events (AEs) and serious adverse events (SAEs) by dose group

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