Phase 1 Myeloma Trial, Recruiting NCT07032714 Sponsor: Massachusetts General Hospital Condition: Myeloma
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Phase 1 Myeloma Trial, Recruiting

NCT07032714
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 given voluntary written consent to take part, with the understanding that they can withdraw at any time without it affecting their future care.
  • People who are reasonably active and able to care for themselves, with a general health/activity score of 2 or below on a standard oncology scale (confirm with trial site).
  • People aged 18 years or older.
  • People who have measurable signs of multiple myeloma in their blood, urine, or through a specific protein level test (confirm with trial site for exact thresholds).
  • People who have already been treated for multiple myeloma with at least three prior rounds of treatment, including specific types of drugs — an immunomodulatory drug, a proteasome inhibitor, and an anti-CD38 antibody — and whose myeloma has come back or stopped responding to treatment within 60 days of their last therapy.
  • People whose blood cell and immune cell counts meet minimum required levels at the time of screening (confirm with trial site for exact values).
  • People whose kidney function meets a minimum threshold, based on a standard kidney function calculation (confirm with trial site).
  • People whose liver function test results are within acceptable ranges at screening (confirm with trial site).
  • People who are able to take blood clot prevention medication, such as aspirin or a similar medicine.
  • Women who could become pregnant must have two negative pregnancy tests before starting treatment and must agree to ongoing pregnancy testing and use of two reliable forms of contraception, or practise complete abstinence, throughout the trial and after it ends.
  • Men must follow the trial's pregnancy prevention plan as outlined by the study team.
  • People who agree to follow specific lifestyle guidelines during the trial, including rules around blood donation, staying near a hospital when required, and avoiding driving or operating heavy machinery when relevant.

Who may not be able to join:

  • People who have received myeloma treatment or an experimental drug within the two weeks before starting the trial, or who are still experiencing side effects from a previous treatment.
  • People who are currently taking part in another clinical trial involving an experimental drug.
  • People who have previously been treated with mezigdomide or iberdomide.
  • People who have previously received a type of treatment targeting a protein called GPRC5D (for example, talquetamab).
  • People who have received a bispecific antibody therapy within the past three months.
  • People who have received gene-modified cell therapy (such as CAR T-cells or NK cells) within the past three months.
  • People who have had plasmapheresis (a procedure to filter the blood) within seven days before starting the trial.
  • People whose myeloma never responded to any treatment from the very beginning (known as primary refractory disease).
  • People who are currently taking high-dose steroid medications for their myeloma (low-dose steroids for unrelated conditions may be acceptable — confirm with trial site).

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 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: Andrew J. Yee, MD, Massachusetts General Hospital

Phone: 617-724-4000

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
19 December 2025
Est. completion
1 July 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Recommended Dose

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