Phase 2 Myeloma Trial, Recruiting NCT04776330 Sponsor: Chongqing Precision Biotech Co., Ltd Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT04776330
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 who have signed a written consent form agreeing to take part
  • People who have been diagnosed with relapsed or refractory multiple myeloma or a related plasma cell disease, and whose cancer either did not respond to standard chemotherapy, came back after going into remission, or came back after a stem cell transplant
  • People whose cancer cells have been shown to carry a specific protein called BCMA on their surface
  • People of any gender aged between 18 and 75 years
  • People whose doctors estimate they are expected to live for more than 3 months
  • People with a general health/performance score above 60 on the KPS scale (a measure of how well someone is functioning day-to-day — confirm with trial site)
  • People with no serious mental health disorders
  • People whose heart is pumping at 50% efficiency or more, as measured by a heart scan
  • People whose liver is functioning within acceptable limits based on blood tests
  • People whose kidneys are functioning within acceptable limits based on blood tests
  • People whose blood oxygen levels are 92% or above while breathing normal indoor air
  • People who are able to have blood or cells collected without medical contraindications
  • People who are willing and able to attend all required trial visits and follow the trial's requirements

Who may not be able to join:

  • People who have a history of another type of cancer
  • People who have an active infection that is not under control
  • People who have a condition that requires ongoing treatment with steroid medications (glucocorticoids)
  • People who have active or chronic graft-versus-host disease (GVHD), a complication that can occur after a stem cell transplant
  • People who are currently being treated with medications that suppress T cell activity (a type of immune cell)
  • People who are pregnant or breastfeeding
  • People with other health or personal circumstances that the trial investigators consider unsuitable for participation, such as HIV, hepatitis C infection, or intravenous drug use, or circumstances that may affect the reliability of the trial 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 21 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: Sanbin Wang, MD, 920th Hospital of Joint Logistics Support Force of People's Liberation Army of China

Phone: 86-13206140093

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
Chongqing Precision Biotech Co., Ltd
Registry
ClinicalTrials.gov
Start date
7 March 2021
Est. completion
31 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Adverse events that related to treatment; The response rate of BCMA targeted prime CAR-T treatment in patients with relapse/refractory Multiple Myeloma that treatment by BCMA targeted prime CAR-T cells therapy

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