Phase 2 Myeloma Trial, Recruiting NCT05900882 Sponsor: The First Affiliated Hospital with Nanjing Medical University Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT05900882
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:

  • People aged 18 to 75 years old
  • People who have been diagnosed with Multiple Myeloma (a type of blood cancer) according to established international guidelines
  • People who are newly diagnosed and whose Multiple Myeloma has spread outside the bone marrow to form tumours (called extramedullary disease), including tumours near bones, in soft tissue, or at other sites — confirmed by scan (CT, MRI, or PET-CT) and/or biopsy, with tumours measuring at least 2cm
  • People whose blood cell counts and platelet levels meet certain minimum levels set by the trial (confirm with trial site for exact values)
  • People whose doctors expect them to live for more than 3 months
  • People who do not have an active infection at the time of joining
  • Women who could become pregnant must have a negative pregnancy test before starting, and all participants must agree to use two reliable forms of contraception for six months after the last dose of study medication
  • People who are willing and able to attend all scheduled visits, follow all treatment plans, and complete all required tests and procedures
  • People who have read, understood, and signed a consent form agreeing to take part in the study

Who may not be able to join:

  • People who have Hepatitis B, Hepatitis C, or other diseases that affect the immune system (either inherited or acquired, such as HIV/AIDS)
  • People who have moderate or severe nerve pain or nerve damage (grade 2 or higher)
  • People who have plasma cell leukaemia (a related but different blood cancer)
  • People who have had serious blood clotting events
  • People with active or unstable heart problems, including chest pain from poor blood flow, uncontrolled heart rhythm problems, significant heart failure, or a heart attack within 3 months before starting the trial
  • People with significantly reduced liver function based on blood test results
  • People with high levels of bilirubin (a substance measured in blood tests that indicates liver or bile issues)
  • People whose kidneys are not filtering blood well enough (below a certain level — confirm with trial site)
  • People who have had another active cancer in the past 5 years, except for certain very early-stage skin or cervical cancers
  • People who have had major surgery within 30 days before starting the trial
  • People who have epilepsy, dementia requiring medication, or other mental health conditions that would make it difficult to follow the study requirements
  • People with serious physical or mental health conditions that, in the doctor's opinion, could interfere with the study
  • People whose personal, family, social, or geographic circumstances might make it difficult to follow the study schedule
  • People who are currently taking part in another clinical trial
  • Women who are pregnant or breastfeeding
  • People with other health conditions that the trial doctors consider unsuitable for participation (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 23 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: Lijuan Chen, The First Affiliated Hospital with Nanjing Medical University

Phone: 025-83714511

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
15 July 2022
Est. completion
30 August 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Number of Participants With 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: 23 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