Phase 2 Myeloma Trial, Recruiting NCT07509086 Sponsor: The First Hospital of Jilin University Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT07509086
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 who are willing and able to give written consent and follow the study schedule, including visits, treatments, and lab tests.
  • People who have been clinically diagnosed with multiple myeloma or plasma cell leukemia that has come back or stopped responding to treatment, or who still have detectable cancer at a very low level (or whose cancer has become detectable again at a very low level) after completing induction and consolidation therapy.
  • People between the ages of 18 and 80 (inclusive).
  • People whose general physical functioning falls within a certain range on a standard medical scale (ECOG score of 0–3, meaning anywhere from fully active to limited in self-care — confirm with trial site).
  • People whose doctors estimate they have a life expectancy of more than 3 months from the time of signing consent.
  • People whose haemoglobin (red blood cell) level is at or above a minimum threshold, including if that level is reached with the help of a blood transfusion.
  • People whose kidneys, heart, lungs, and liver are functioning at or above certain minimum levels as determined by standard tests (confirm specific thresholds with trial site).
  • People who are capable of becoming pregnant, or whose partners are capable of becoming pregnant, who agree to use effective contraception from before joining the study until at least 6 months after treatment ends, and who agree to notify the study team immediately if pregnancy occurs or is suspected.

Who may not be able to join:

  • People who, within the past year, have had serious heart conditions such as severe heart failure, a heart attack, a procedure to open blocked heart arteries (angioplasty or stent), unstable chest pain (angina), or other significant symptomatic heart disease.
  • People who currently have active graft-versus-host disease (a complication sometimes seen after stem cell transplants) or who need ongoing medication to suppress their immune system.
  • People who have had another type of cancer within the past 5 years, with some exceptions for certain early-stage or fully treated skin cancers, cervical pre-cancers, localised prostate cancer after surgery, or early breast cancer after curative surgery (confirm with trial site).
  • People who have an active infection requiring treatment with systemic medication, or who had an uncontrolled infection within the 7 days before screening (minor urinary or upper respiratory infections may be exceptions — confirm with trial site).
  • People who test positive for certain infectious diseases, including active hepatitis B, active hepatitis C, HIV, or syphilis.
  • People who have participated in another clinical trial within the past 4 weeks, or whose last dose of an experimental drug was less than 5 half-lives ago — whichever period is longer.
  • People who have a history of severe allergic reactions to biological medicines (such as antibody-based therapies).
  • People who have any unstable or serious ongoing illness affecting the liver, kidneys, or metabolism that requires medical treatment, as determined by the investigating doctor.
  • People who are pregnant or breastfeeding, people who plan to become pregnant within 2 years after receiving the cell treatment, or male participants whose partners plan to become pregnant within 2 years after their cell treatment.
  • People who have any other condition that the investigating doctor believes could increase risk or interfere with the study.

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 22 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
The First Hospital of Jilin University
Registry
ClinicalTrials.gov
Start date
29 December 2025
Est. completion
15 July 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

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: 22 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