Phase 3 Myeloma Trial, Recruiting NCT06879379 Sponsor: Peking University People's Hospital Condition: Myeloma
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Phase 3 Myeloma Trial, Recruiting

NCT06879379
Recruiting Phase 3

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 are 18 years of age or older.
  • You have been recently diagnosed with multiple myeloma (MM) and are eligible to receive a stem cell transplant.
  • You received an initial treatment regimen using three or four drugs (triplet or quadruplet therapy).
  • You received your own stem cell transplant (known as an autologous stem cell transplant) after that initial treatment.
  • You are generally active and able to care for yourself, with only minor limitations on physical activity (confirm with trial site).
  • Your liver is functioning well, based on specific blood test results being within acceptable ranges.
  • Your heart is pumping effectively (at least 50% efficiency), with no significant heart rhythm problems shown on a heart tracing test.
  • Your blood oxygen level is above 95% while breathing normal room air.
  • Women who could become pregnant agree to use effective birth control during the study and for at least 3 months after the last dose of the study drug, followed by highly effective birth control for at least one year after that.
  • Men with partners who could become pregnant agree to use barrier contraception (such as condoms) during the study and for at least 3 months after the last dose.
  • You are willing and able to follow the study procedures and have signed a consent form agreeing to take part.

Who may not be able to join:

  • You have been diagnosed with a related but different blood condition, such as plasma cell leukemia, POEMS syndrome, primary amyloidosis, Waldenström's macroglobulinemia, monoclonal gammopathy of undetermined significance (MGUS), or smoldering multiple myeloma.
  • You have a serious mental health condition, changes in mental awareness, or a history of brain or nervous system conditions such as epilepsy, stroke, dementia, or certain autoimmune diseases affecting the brain or nervous system.
  • You have a history of certain inherited genetic conditions affecting the bone marrow, such as Fanconi anemia, Shwachman-Diamond syndrome, or Costello syndrome (confirm with trial site for full list).
  • You were diagnosed with or treated for another type of cancer within the past year, or you have any remaining signs of a previous cancer (with some exceptions for certain skin cancers or fully removed early-stage cancers).
  • You currently have an active infection, are known to be HIV-positive, or have an active hepatitis B or C infection.
  • You have a known allergy to any of the study drugs or their ingredients.
  • There is any sign or suspicion that your myeloma has spread to the brain or spinal fluid.
  • You have a drug use issue, or medical, psychological, or social circumstances that could interfere with your ability to take part in the study.
  • You are currently pregnant or breastfeeding.
  • The trial doctor considers you unsuitable for the trial for any other reason.

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 2 July 2026
Phase 3: approximately ~65% 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.

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Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
Peking University People's Hospital
Registry
ClinicalTrials.gov
Start date
1 March 2025
Est. completion
1 March 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Minimal residual disease (MRD) negativity rate prior to maintenance therapy; Overall Response Rate (ORR)

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: 2 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