Phase 1 Myeloma Trial, Recruiting NCT07529782 Sponsor: Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd. Condition: Myeloma
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Phase 1 Myeloma Trial, Recruiting

NCT07529782
Recruiting 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:

  • People aged 18 or older, of any gender.
  • People who are expected to live for more than 12 weeks.
  • People who are reasonably active or able to care for themselves, based on a standard cancer performance scale scored 0 to 2 (confirm with trial site).
  • People who have a confirmed diagnosis of active multiple myeloma, as defined by international myeloma guidelines.
  • People who have previously had a stem cell transplant, or who have been assessed as not suitable for a stem cell transplant.
  • People who have already received at least three types of myeloma treatment — specifically, an immunomodulatory drug, a proteasome inhibitor, and an anti-CD38 treatment — and whose myeloma has stopped responding to, or who could not tolerate, standard available treatments.
  • People whose myeloma can be measured through standard testing (with some flexibility in the dose-escalation part of the trial for those with a form of myeloma that produces little or no detectable protein).
  • People whose heart, liver, kidneys, and other organs are functioning at a level that meets the trial's health requirements (confirm specific thresholds with trial site).

Who may not be able to join:

  • People whose myeloma has spread to the central nervous system (brain or spinal cord).
  • People who have plasma cell leukaemia.
  • People with a history of heart failure.
  • People who have had a stem cell transplant (either using their own cells or a donor's cells) within the 12 weeks before the trial starts, or who are planning to have a stem cell transplant using their own cells.
  • People who have had significant graft-versus-host disease within the 12 months before the trial starts, following a donor stem cell transplant.
  • People who have received radiotherapy within 21 days before the trial starts.
  • People with a history of another active cancer.
  • People with a known HIV infection.
  • People who currently have an active infection requiring treatment with antibiotics, antivirals, or similar medicines.
  • People with an active hepatitis B or hepatitis C infection.
  • People with a currently active liver or bile duct disease.
  • People who are pregnant or breastfeeding.
  • People who currently have pneumonia or inflamed lungs causing symptoms.

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 26 July 2026
Phase 1: approximately ~10% 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

Phone: +8618428347838

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 1
Sponsor
Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.
Registry
ClinicalTrials.gov
Start date
17 March 2026
Est. completion
30 June 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Number of patients who experience a dose-limiting toxicity (DLT) during the first cycle of treatment.

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: 26 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