Phase 1 Myeloma Trial, Recruiting NCT07620275 Sponsor: Chinese PLA General Hospital Condition: Myeloma
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Phase 1 Myeloma Trial, Recruiting

NCT07620275
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 to 75 years of any gender
  • People who have a confirmed diagnosis of multiple myeloma that has come back or stopped responding to treatment, and who have already received at least 3 previous treatment regimens (including at least one type from each of two specific drug classes: a proteasome inhibitor and an immunomodulatory agent)
  • People whose myeloma got worse during or within 12 months after their most recent treatment, or whose myeloma got worse within the last 6 months and did not respond to the most recent treatment
  • People who the treating doctor considers unable to tolerate standard treatments may also be considered
  • People whose myeloma can be measured at the time of screening through specific protein levels in the blood or urine, or through certain blood markers for a particular type of myeloma
  • People whose myeloma cells test positive for certain proteins called CD19 and/or BCMA (confirmed by laboratory testing of tumour tissue; previous test results may be accepted in some cases, but a new biopsy may be needed if prior treatment targeted these proteins)
  • People whose side effects from previous treatments have mostly settled, with any remaining side effects being mild (Grade 1 or lower), apart from certain blood-related effects or minor issues like hair loss
  • People who are reasonably well and able to carry out daily activities, as measured by a standard medical scale (ECOG score of 0, 1, or 2)

Who may not be able to join:

  • People whose life expectancy is estimated to be less than 3 months
  • People who have, or have had, another active cancer — though some exceptions may apply, such as certain treated skin cancers, cervical changes that have been fully treated with no recurrence for at least 3 years, locally treated prostate cancer, or certain fully surgically treated breast conditions (confirm with trial site)
  • People who have had a stem cell transplant using donor cells at any time, or their own cells within the past 3 months before the planned trial treatment
  • People whose myeloma is present only as a single soft tissue growth outside the bone marrow
  • People diagnosed with certain related blood or plasma cell conditions, including plasma cell leukaemia, Waldenström's macroglobulinaemia, POEMS syndrome, or primary AL amyloidosis
  • People who have cancer that has spread to the brain or spinal fluid, or who have symptoms suggesting this
  • People who have recently received other anti-cancer treatments and whose body has not yet cleared those treatments (within 5 half-lives of that treatment before the planned trial treatment date)
  • People who have an active infection that is not under control
  • People who test positive for HIV, syphilis, or certain hepatitis B or C markers with detectable virus levels in the blood — though exceptions may apply if the treating doctor considers the infection preventable or controllable with medication
  • People with a known active autoimmune disease that requires ongoing treatment affecting the whole body
  • People with a known serious allergic reaction to the study drug or any of its ingredients
  • People who are pregnant or breastfeeding
  • People who have received a live vaccine within 6 weeks before enrolling in the trial

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 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: +86-010-55499341

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
Chinese PLA General Hospital
Registry
ClinicalTrials.gov
Start date
10 June 2026
Est. completion
15 December 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Dose limited toxicity (DLT); Incidence and severity of AEs and serious adverse events (SAEs); Incidence and severity of adverse events of special interest (AESI)

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