Early Phase 1 Myeloma Trial, Recruiting NCT04662294 Sponsor: Zhejiang University Condition: Myeloma
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Early Phase 1 Myeloma Trial, Recruiting

NCT04662294
Recruiting Early Phase 1

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:

For people with Acute Myeloid Leukemia (AML):

  • A diagnosis of AML that has been confirmed through laboratory tissue testing, and the cancer cells carry a specific protein called CD70
  • The AML has come back or stopped responding to treatment, meaning either: standard chemotherapy did not achieve remission; remission was achieved but lasted less than 12 months; one or more follow-up treatments did not work; or the cancer has relapsed two or more times
  • Bone marrow test results show a certain level of abnormal (blast) cells above set thresholds (confirm with trial site for exact values)
  • Liver and kidney function blood test results that fall within acceptable ranges set by the trial
  • A heart scan (echocardiogram) showing the heart is pumping at 50% or more of its normal capacity
  • No active lung infection, and blood oxygen levels at or above 92% while breathing normal indoor air
  • A life expectancy estimated at 3 months or more
  • A general health and activity level score of 0, 1, or 2 on a standard medical scale (meaning able to carry out at least some daily activities)
  • Willingness to take part and ability to sign a consent form (a legal guardian may sign on behalf of the patient if needed)

For people with Non-Hodgkin Lymphoma (NHL):

  • People of any gender and age may be considered
  • A confirmed diagnosis of one of the following specific types of lymphoma, identified through laboratory tissue testing: DLBCL (NOS), Follicular Lymphoma, DLBCL transformed from CLL/SLL, Primary Mediastinal B-Cell Lymphoma, or High-Grade B-Cell Lymphoma, and the cancer cells carry the CD70 protein
  • The lymphoma has come back or stopped responding to treatment, meaning either: no response or relapse after at least two lines of chemotherapy; the cancer showed resistance to treatment from the start; or relapse occurred after a stem cell transplant using the patient's own cells
  • At least one measurable area of disease visible on scans, assessed using a standard set of lymphoma measurement guidelines

For people with Multiple Myeloma (MM):

  • A confirmed diagnosis of multiple myeloma that carries the CD70 protein, and the disease meets one of the following: it has returned or stopped responding to treatment according to international myeloma guidelines; there are detectable traces of disease remaining after treatment; or there is disease outside the bone marrow that has been difficult to clear with chemotherapy or radiation
  • People of any gender and age may be considered
  • Liver and kidney function blood test results that fall within acceptable ranges set by the trial
  • A heart scan (echocardiogram) showing the heart is pumping at 50% or more of its normal capacity
  • No active lung infection, and blood oxygen levels at or above 92% while breathing normal indoor air
  • A life expectancy estimated at 3 months or more
  • A general health and activity level score of 0, 1, or 2 on a standard medical scale
  • Willingness to take part and ability to sign a consent form (a legal guardian may sign on behalf of the patient if needed)

Who may not be able to join:

  • People with a history of serious brain or nervous system conditions, including head injury, loss of consciousness, epilepsy, stroke, or bleeding in the brain
  • People with a history of a prolonged QT interval on a heart tracing (ECG), or other serious heart rhythm problems
  • People who are pregnant or breastfeeding
  • People with a severe active infection (minor infections such as a urinary tract infection or throat infection caused by bacteria may not automatically disqualify someone — confirm with trial site)
  • People with an active hepatitis B or hepatitis C infection
  • People who have been taking steroid tablets or injections throughout the body within the 2 weeks before screening, unless the steroids are inhaled (such as for asthma)
  • People who have previously received any CAR-T cell therapy or other gene-modified T cell treatments
  • People whose liver or kidney function blood test results fall outside acceptable limits set by the trial
  • People with other serious uncontrolled health conditions that the trial team considers unsuitable (confirm with trial site)
  • People living with HIV
  • Any other situation that the trial investigators believe could put the patient at increased risk or affect the reliability of the trial results (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 14 July 2026
Early Phase 1 studies are small, early exploratory studies that come before the main Phase 1 to 3 testing, so a standard phase success rate does not apply.

Contact this trial

Phone: 86-13605714822

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
Early Phase 1
Sponsor
Zhejiang University
Registry
ClinicalTrials.gov
Start date
18 November 2021
Est. completion
15 January 2024

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Dose-limiting toxicity (DLT); Incidence of treatment-emergent adverse events (TEAEs)

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: 14 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