Clinical trial No longer in our active list Interventional Ages 18 to 70

Management scheme for patients with multiple myeloma and renal injury

Official title: A Clinical Study on the Whole-course Management (BCD-KPD-AutoHSCT) Scheme for Patients With Multiple Myeloma and Kidney Injury

Run by Peking University First Hospital · NCT06203145 · Data updated 2026-05-14

This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.

This study tests a new treatment plan for people with multiple myeloma and kidney problems to see if early chemotherapy and stem cell transplants can help improve their kidney function and overall health.

More Multiple Myeloma trials

Quick facts

Study typeInterventional
Ages18 Years to 70 Years
SexAll
Enrollment30 (estimated)
SponsorPeking University First Hospital
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Beijing, Beijing)
Trial IDNCT06203145 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults aged 18 and older with a confirmed diagnosis of symptomatic multiple myeloma and renal impairment.

Probably not a fit

Patients with chronic kidney disease unrelated to myeloma or other severe co-existing medical conditions may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical study investigates a comprehensive management approach for patients suffering from multiple myeloma with renal impairment. It focuses on the effects of early intensive chemotherapy and autologous hematopoietic stem cell transplantation (AutoHSCT) on reversing renal function in these patients. The study aims to evaluate the treatment outcomes based on different renal pathological types associated with multiple myeloma. By utilizing established drug regimens, the research seeks to improve survival rates and quality of life for affected individuals.

Why it matters

Potential benefit: If successful, this study could significantly improve renal function and survival rates in patients with multiple myeloma and renal injury.

How similar studies have gone: Other studies have shown promising results with similar approaches in treating multiple myeloma, particularly regarding the management of renal complications.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Adults aged 18 years or older
2. Confirmed diagnosis of symptomatic myeloma with renal impairment
3. Confirmed myeloma-associated nephropathy (e.g. light chain cast nephropathy, AL amyloidosis, MIDD etc.) on renal biopsy
4. Willingness and eligibility for autologous hematopoietic stem cell transplantation

Exclusion Criteria:

1. Pre-existing chronic kidney disease unrelated to myeloma, such as diabetic nephropathy or hypertensive nephropathy
2. Plasma cell leukemia or extramedullary plasmacytoma
3. Contraindications or prior severe allergic reactions to study medications
4. Co-existing malignancy
5. Co-existing medical conditions unsuitable for enrollment as determined by researchers, such as recent cardiovascular event, active infection etc.

Where it's running

  • Peking University First Hospital
    Beijing, Beijing, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.