Phase 2 Myeloma Trial, Recruiting NCT07585760 Sponsor: Institute of Hematology & Blood Diseases Hospital, China Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT07585760
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 aged 18 to 80 years
  • People who have been newly diagnosed with multiple myeloma that is causing symptoms, based on internationally recognised diagnostic criteria
  • People who have received at most one cycle of treatment for multiple myeloma before enrolling, as long as that treatment did not include immunotherapy
  • People whose myeloma can be measured through at least one of the following: a specific abnormal protein detected in the blood at a certain level; an abnormal protein detected in urine over a 24-hour collection; or an abnormal balance of certain protein fragments in the blood (confirm with trial site for exact thresholds)
  • People whose myeloma has caused kidney damage of a specific type — where the kidneys are being harmed by protein casts blocking the kidney tubes — with kidney function below a certain threshold as measured by a standard formula; a kidney biopsy may be required to confirm this in some cases (confirm with trial site)
  • People whose general physical health and ability to carry out daily activities falls within an acceptable range on a standard medical scoring scale (a score of 0, 1, or 2 on the ECOG scale)
  • People whose blood cell counts, liver function, and blood clotting results meet the minimum levels required by the trial (confirm with trial site for specific values)
  • People who do not have another active cancer, or whose other cancer is not expected to affect survival within the next 12 months
  • People who are willing to participate, able to follow the study requirements, and able to provide signed consent

Who may not be able to join:

  • People diagnosed with related but distinct conditions such as smoldering myeloma, MGUS, Waldenström's macroglobulinemia, POEMS syndrome, amyloidosis, or secondary plasma cell leukaemia
  • People whose myeloma or cancer has spread to the brain or the fluid surrounding the brain and spine
  • People with serious or poorly controlled heart conditions, including unstable chest pain, heart failure with symptoms, a heart attack within the past 6 months, severe irregular heartbeat, or other heart or stroke-related conditions the trial doctor considers unsuitable
  • People with active infections, including HIV, active hepatitis B, active hepatitis C, active or latent syphilis, active tuberculosis detected in the past 3 months or during screening, or other active infections the trial doctor considers unsuitable
  • People with another cancer occurring at the same time, or with serious other health conditions that could put their safety at risk or interfere with completing the trial
  • People who are pregnant or breastfeeding
  • People who have previously had a severe allergic reaction (grade 3 or higher) to any ingredient in the study medications
  • People who are unwilling or unable to sign the consent form
  • People who, in the trial doctor's judgement, are unsuitable for any other reason

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 27 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.

Contact this trial

Phone: +86 13502181109

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 2
Sponsor
Institute of Hematology & Blood Diseases Hospital, China
Registry
ClinicalTrials.gov
Start date
25 July 2026
Est. completion
1 May 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Overall Renal Response Rate (Minor Response or better)

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: 27 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