Phase 1 Myeloma Trial, Recruiting NCT06185751 Sponsor: Washington University School of Medicine Condition: Myeloma
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Phase 1 Myeloma Trial, Recruiting

NCT06185751
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:

  • You have multiple myeloma that has come back or stopped responding to treatment, and you have already tried at least 3 different types of treatment, including specific drug types targeting myeloma in different ways (such as bortezomib or carfilzomib, daratumumab, and a BCMA-targeted therapy).
  • Your myeloma can be measured through at least one blood test, urine test, bone marrow sample, or biopsy showing the disease is still active.
  • You are at least 18 years old.
  • You are generally well enough to carry out light activity and care for yourself (confirm with trial site what this means for your situation).
  • Your kidneys, liver, lungs, and heart are all working well enough to meet specific tested levels (confirm with trial site for exact details).
  • If you can become pregnant, or if your partner can become pregnant, you must agree to use at least 2 forms of contraception — including one barrier method — starting before joining the trial and continuing for 12 months after treatment.
  • You are able to understand the trial and willing to sign a consent form agreeing to take part.

Who may not be able to join:

  • You have received any myeloma treatment within the 14 days before the planned cell collection procedure.
  • You have a history of another cancer, unless it was a treated skin cancer (non-melanoma) or a cancer that was fully treated at least 2 years ago with no signs of return.
  • You are currently taking part in another clinical trial using an experimental treatment.
  • You have received a cell-based therapy within the 8 weeks before the planned start of the preparatory treatment for this trial.
  • You have had a serious allergic reaction to treatments similar to the one being studied (confirm with trial site).
  • You have previously had a severe reaction (Grade 3 or higher) to another CAR-T cell therapy, including BCMA CAR-T treatments.
  • You currently have active hepatitis B, active hepatitis C, HIV, or any infection that is not under control.
  • You have an ongoing infection or other serious health condition that could make it unsafe to receive the trial treatment.
  • You are pregnant or breastfeeding; women who could become pregnant must have a negative pregnancy test within 14 days of starting 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 14 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: Armin Ghobadi, M.D., Washington University School of Medicine

Phone: 314-747-2743

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
Registry
ClinicalTrials.gov
Start date
22 August 2024
Est. completion
31 August 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Part A: Frequency and severity of treatment-emergent adverse events; Part A: Frequency of dose-limiting toxicities (DLTs); Part B: Frequency and severity of treatment-emergent adverse events

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: 14 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