Phase 2 Myeloma Trial, Recruiting NCT05632380 Sponsor: Institute of Hematology & Blood Diseases Hospital, China Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT05632380
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:

  • Adults between 18 and 65 years old who are considered suitable candidates for a stem cell transplant
  • People diagnosed with very high-risk multiple myeloma whose disease either did not respond well enough, or stopped responding, to a standard first-line treatment regimen (VRD-based therapy), with or without certain high-risk genetic features in their cancer cells
  • People whose liver, kidneys, bone marrow, and heart are functioning at an adequate level
  • People who are generally well enough to carry out daily activities with little to no limitation (based on a standard medical fitness scale called ECOG, scoring 0 or 1)
  • People who are capable of having children and who agree to use contraception throughout the study period

Who may not be able to join:

  • People with a known allergy to any ingredient in the C-CAR088 cell treatment being studied
  • People who have previously had a donor stem cell transplant or their own stem cell transplant
  • People whose multiple myeloma has spread to the central nervous system (brain or spinal cord)
  • People who have had a stroke or seizure within the 6 months before signing the study consent form
  • People with an autoimmune disease, a weakened immune system, or any condition that requires them to take immune-suppressing medications
  • People with an active infection that is not under control, or an active hepatitis B, hepatitis C, HIV, or syphilis infection
  • People with serious heart, liver, kidney, or metabolic disease
  • People who have not waited long enough after their last cancer treatment before the cell collection process (apheresis) can take place
  • People who have previously received CAR-T cell therapy, other genetically modified T-cell treatments, or any treatment targeting a protein called BCMA
  • People with any other medical condition, ongoing therapy, or abnormal test result that, in the investigator's judgement, could affect the safety or results of the trial

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 27 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: Dehui Zou, M.D., PH.D., Institute of Hematology & Blood Diseases Hospital, China

Phone: 86-022-23909171

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
Institute of Hematology & Blood Diseases Hospital, China
Registry
ClinicalTrials.gov
Start date
14 July 2022
Est. completion
30 October 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence rate and severity of adverse events (AE)

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: 27 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