Phase 2 Myeloma Trial, Recruiting NCT06483100 Sponsor: Washington University School of Medicine Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT06483100
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 are at least 18 years old
  • People who are able to understand and willing to sign a consent form (a legal representative may sign on their behalf if needed)
  • People who have been diagnosed with a specific type of multiple myeloma (called IgG or IgA multiple myeloma) and have received a stem cell transplant using their own cells (called an autologous transplant) as part of their first course of treatment
  • People whose first course of treatment included at least three cancer medicines, including specific drug types known as a PI and an IMID, with or without an anti-CD38 antibody medicine
  • People whose myeloma has responded at least partially to treatment, based on standard measurement criteria, at the time of joining the study
  • People whose myeloma is still detectable at a low level (called MRD-positive) on a specialised bone marrow test done around 100 days after their stem cell transplant
  • People who are generally well enough to carry out light activity and care for themselves (assessed using a standard health scale)
  • People whose side effects from previous treatment have mostly resolved to a mild level before joining
  • People whose blood counts and organ function (bone marrow, liver, and kidneys) meet specific minimum levels within 28 days before starting treatment
  • People of childbearing potential and male participants who agree to use reliable contraception during the study and for 5 months after treatment ends

Who may not be able to join:

  • People whose myeloma cells cannot be tracked using the specific laboratory test (clonoSEQ) required by this trial
  • People who have had another type of cancer, with some exceptions: non-melanoma skin cancers, certain low-risk prostate cancers, and cancers for which all treatment was completed at least 2 years ago with no signs of disease remaining (hormone therapy for breast cancer is also not disqualifying)
  • People who are currently taking part in another clinical trial involving an experimental treatment
  • People who have previously received a treatment that targets a protein called BCMA
  • People whose myeloma has spread to the brain or spinal cord
  • People who have had a serious allergic reaction to medicines similar to the study drug (elranatamab)
  • People with certain serious or uncontrolled conditions, including plasma cell leukemia, POEMS syndrome, systemic amyloidosis, or an active ongoing infection
  • People who are pregnant or breastfeeding; women of childbearing potential must have a negative pregnancy blood test within 28 days before starting the study drug
  • People living with HIV who are not on effective HIV treatment or who have not had an undetectable level of virus in their blood for at least the past 6 months

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 12 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: Michael Slade, M.D., Washington University School of Medicine

Phone: 314-454-8304

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
Registry
ClinicalTrials.gov
Start date
20 December 2024
Est. completion
31 December 2031

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Progression-free survival (PFS); Proportion of patients achieving MRD negativity at the 10^-5 threshold per the clonoSEQ assay

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: 12 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