Phase 2 Myeloma Trial, Recruiting NCT06376526 Sponsor: Dickran Kazandjian, MD Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT06376526
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:

  • You have been newly diagnosed with multiple myeloma (a type of blood cancer), confirmed before any treatment began.
  • You have already received a combination of three or four drugs to treat your myeloma, including at least two from these groups: immunomodulatory drugs (IMiDs), proteasome inhibitors (PIs), and/or anti-CD38 drugs.
  • After at least 4 rounds of that combination treatment, your cancer responded very well, but a very sensitive test still detected some remaining cancer cells.
  • You are 18 years of age or older.
  • You are generally able to care for yourself and are up and about for most of the day (your doctor can help assess this).
  • Your blood counts, liver, and kidneys are working at an acceptable level, as shown by blood tests (your trial team will check this).
  • If you are a woman who could become pregnant, you have had a negative pregnancy test before starting the trial.
  • You are willing and able to use highly effective birth control during the trial and for 6 months after your last dose of the study treatment.
  • You are willing and able to attend clinic visits and follow the study procedures.
  • You are able to give written consent to take part.

Who may not be able to join:

  • You have received other treatments for your myeloma beyond the initial combination therapy described above, including a stem cell transplant (your own or a donor's).
  • You are currently taking part in another clinical trial using an investigational (experimental) drug.
  • You have received a live vaccine within 4 weeks before your scheduled start of study treatment.
  • You have a known allergy or serious reaction to any of the medications used in this trial.
  • You are HIV-positive and also have a low immune cell count, a detectable level of HIV in your blood, are not on appropriate HIV treatment, or your HIV medication may interfere with the study drugs (confirm with trial site).
  • You have an active hepatitis B infection, or testing shows hepatitis B virus is still present in your blood.
  • You have an active hepatitis C infection (detectable virus in your blood), unless you have completed treatment for it and the virus is no longer detectable.
  • You are a woman who is breastfeeding and are unwilling to stop during treatment or for 6 months after your last dose.
  • You are unwilling to use highly effective contraception during the trial and for at least 6 months after your last dose.
  • You have significant heart problems, such as severe heart failure, a heart attack or heart bypass surgery within the past 6 months, serious irregular heartbeat, or unstable heart disease.
  • You have another serious uncontrolled illness, such as an active infection, active autoimmune disease, a blood clot condition, serious lung problems, or a psychiatric condition that could prevent you from following the study requirements.
  • You have had another type of cancer requiring treatment within the past 12 months (some exceptions may apply — confirm with trial site).
  • You have any other condition that, in the doctor's judgment, could put you at risk or prevent you from completing the trial.
  • You are not able to make your own medical decisions.

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 28 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: Dickran Kazandjian, MD, University of Miami

Phone: 305-243-5001

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
Dickran Kazandjian, MD
Registry
ClinicalTrials.gov
Start date
21 August 2024
Est. completion
31 August 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Minimal Residual Disease (MRD) Negativity Rate

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: 28 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