Phase 2 Myeloma Trial, Recruiting NCT06679829 Sponsor: Memorial Sloan Kettering Cancer Center Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT06679829
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 diagnosed with multiple myeloma (confirmed by a tissue test) with symptoms, and you are planning to have a stem cell transplant using your own stem cells, with a specific chemotherapy drug (melphalan) as part of that process, within 12 months of your diagnosis
  • You are at least 60 years old
  • You have enough stem cells collected and ready to be used (at least 3 million of a specific type called CD34+ cells per kg of body weight)
  • You are in reasonably good general health, able to carry out most daily activities (confirm with trial site for exact fitness level required)
  • Your lungs are working at more than 45% of expected capacity, based on a breathing test done within the past 6 weeks
  • Your heart is pumping at more than 45% efficiency, based on a heart scan done within the past 6 weeks
  • Your recent blood test results (within the past 6 weeks) show your platelet count, liver function, and kidney function are all above certain minimum levels (confirm with trial site for exact values)
  • If you are a man who is sexually active with a woman who could become pregnant, you must agree to use a barrier form of contraception (such as a condom) during the study and for 3 months after your last dose, and must not donate sperm during this time

Who may not be able to join:

  • You have previously been treated with drugs that target a substance called IL-6 or its receptor
  • You have had another type of cancer in the past 2 years, with some exceptions for certain treated and inactive skin or cervical cancers (men with prostate cancer being monitored but not treated may be considered — confirm with trial site)
  • You have another medical condition (such as an autoimmune disease or active infection) that could interfere with the study or make participation unsafe
  • You have had a heart problem requiring treatment in the last 3 months, or you have uncontrolled heart failure or an uncontrolled irregular heartbeat, or your heart's electrical activity reading is outside of a safe range (confirm with trial site)
  • You have received a live vaccine within 4 weeks before starting the study
  • You have a significant active infection, or are known to have HIV, hepatitis C, or hepatitis B, unless certain conditions are met showing the infection is under control (confirm with trial site for details)
  • You have taken part in another clinical trial or used an experimental treatment or device within the past 14 days (or within 5 half-lives of that drug) before joining, or are currently in the treatment phase of another study
  • You were hospitalised for an infection or had major surgery requiring general anaesthesia within the 2 weeks before joining, or have not fully recovered from surgery
  • You are a man who plans to father a child while on the study or within 3 months after your last dose of the study drug

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: Gunjan Shah, MD, MS, Memorial Sloan Kettering Cancer Center

Phone: 646-608-3734

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
6 November 2024
Est. completion
1 November 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

rate of stringent complete response (sCR)

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