Myeloma Trial, Recruiting NCT06463717 Sponsor: First Affiliated Hospital of Zhejiang University Condition: Myeloma
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Myeloma Trial, Recruiting

NCT06463717
Recruiting Not Applicable

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 been newly diagnosed with multiple myeloma, based on internationally recognised diagnostic guidelines
  • People between 18 and 70 years of age
  • People whose myeloma showed a very strong response to 4–6 rounds of initial treatment, including reaching a level where cancer cells are extremely difficult to detect using a highly sensitive laboratory test
  • People whose general physical functioning is rated as good to mildly limited at the time of enrolling (rated 0–2 on a standard medical scale)
  • People whose liver, kidney, and heart are functioning within acceptable ranges as measured by specific blood and heart tests (confirm specific values with the trial site)
  • People who are expected to survive for more than 3 months

Who may not be able to join:

  • People who have two or more high-risk genetic changes in their myeloma cells, as identified by a specific chromosome analysis test (confirm details with the trial site)
  • People whose myeloma has spread outside the bone marrow, affected the central nervous system, or developed into plasma cell leukaemia
  • People who have had another cancer in the past 5 years
  • People living with HIV, active tuberculosis, or currently active hepatitis A, B, or C
  • People with serious ongoing health conditions such as severe infection, uncontrolled diabetes, significant heart failure, or unstable chest pain
  • People whose overall health is considered unsuitable for chemotherapy
  • People who are pregnant or breastfeeding
  • People with serious disease affecting other organs, or serious mental health disorders

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 12 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Haitao Meng, Zhejiang University

Phone: +86 15088687797

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
Not Applicable
Sponsor
First Affiliated Hospital of Zhejiang University
Registry
ClinicalTrials.gov
Start date
1 December 2023
Est. completion
1 November 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

progression free survival

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: 12 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