Phase 1 Myeloma Trial, Recruiting NCT06523699 Sponsor: Washington University School of Medicine Condition: Myeloma
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Phase 1 Myeloma Trial, Recruiting

NCT06523699
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 who have been confirmed with a diagnosis of multiple myeloma according to established international guidelines (IMWG criteria).
  • People whose multiple myeloma is currently in a first complete response (full or stringent), or has partially responded or responded very well to treatment, as measured by IMWG guidelines.
  • People whose treating doctor considers them a suitable candidate for a stem cell transplant using their own cells (autologous transplant) with a chemotherapy drug called melphalan.
  • People aged 18 or older.
  • People who are reasonably active and able to care for themselves, based on a standard medical fitness scale (ECOG score of 0, 1, or 2).
  • People whose bone marrow and major organs (liver and kidneys) are functioning well enough to meet specific blood test thresholds set by the trial.
  • People who are willing and able to use reliable contraception (hormonal, barrier, or abstinence) before joining the trial and for one year after transplant — this applies to both women who could become pregnant and men. Anyone who suspects a pregnancy has occurred during this time must inform their treating doctor immediately.
  • People who are able to understand and are willing to sign an informed consent form approved by an ethics review board (or have a legal representative do so on their behalf).

Who may not be able to join:

  • People who have taken high doses of corticosteroids (more than the equivalent of 5 mg of prednisone per day) within two weeks before the trial begins, except when used as part of a stem cell collection preparation (mobilization regimen).
  • People with a history of T-cell blood cancer, plasma cell leukaemia, amyloidosis, or another cancer — unless it was a non-invasive skin cancer, a non-melanoma skin cancer, or a cancer for which all treatment was completed at least two years before the trial starts with no signs of the disease remaining.
  • People who are currently taking part in another clinical trial involving an experimental treatment.
  • People who have had a significant allergic reaction to drugs that are chemically or biologically similar to any of the treatments used in this trial, including CYT107 or melphalan.
  • People who have taken certain immune-suppressing medications (azathioprine, methotrexate, or anti-TNF agents) within two weeks before the trial begins.
  • People with a history of a congenital (inherited) immune deficiency condition, or an autoimmune disease — though people whose autoimmune condition is well controlled on a low dose of medication (5 mg prednisone equivalent or less per day) may still be considered.
  • People with a history of significant lung problems, such as severe asthma, severe chronic obstructive pulmonary disease (COPD), restrictive lung disease, a blood clot in the lungs within the past three months, or any active or prior inflammatory lung condition.
  • People with serious uncontrolled health conditions, including active infections, heart failure, unstable chest pain, or irregular heart rhythms.
  • People who are pregnant or breastfeeding. Women who could become pregnant must have a negative pregnancy test within seven days before the trial begins.
  • People who do not have a backup supply of their own stem cells available.

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 13 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: Dilan A Patel, M.D., Washington University School of Medicine

Phone: 314-747-8173

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
4 April 2025
Est. completion
30 April 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Rate of non-hematologic grade ≥3 CYT107 treatment-related AEs (excluding expected transplant-related AEs or AEs attributed to melphalan and ASCT) according to CTCAE v5

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: 13 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