PLUMM Study: Mycophenolate Mofetil for Lupus Nephritis in Children

This study, called PLUMM, is looking at two different ways to give a medicine called Mycophenolate Mofetil (MMF) to children and young adults (ages 8 to 20) with lupus nephritis. Lupus nephritis is a kidney condition caused by lupus. One way of giving MMF is based on body size, and the other is a more personalized approach based on how your body processes the medicine. The study wants to see which method is more effective at treating lupus nephritis after 26 weeks. To join, you must have lupus and a recent diagnosis of proliferative lupus nephritis confirmed by a kidney biopsy. The study is currently recruiting participants.

Study design
This is a double-blinded study with two groups, meaning neither you nor your doctor will know which MMF dosing method you are receiving. It plans to enroll 105 participants.
What's involved
You would receive blinded treatment for up to 53 weeks. You would also have study visits at weeks 26 and 53/End of Study.
Compensation
Not stated in the trial record.
Follow-up
The primary goal is measured at 26 weeks, and the study continues for up to 53 weeks.

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NCT05538208

The Pediatric Lupus Nephritis Mycophenolate Mofetil (PLUMM) Study

Recruiting
PHASE2Ages 8–20InterventionalTreatment
Children's Hospital Medical Center, Cincinnati
~105 participants
Updated 2026-03-18 on ClinicalTrials.gov
What's tested:Mycophenolate Mofetil

At a glance

Recruiting sites
19 of 19 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
To compare the efficacy of MMFPK therapy to the efficacy of MMFBSA therapy
Measured over 26 week
Lupus Nephritis
19 sites across 14 states
Ohio4
Illinois2
New York2
California1
Colorado1
Georgia1
Missouri1
New Jersey1
  • Hermine I Brunner, MD · PRINCIPAL_INVESTIGATOR · Children's Hospital Medical Center, Cincinnati

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  • To compare the efficacy of MMFPK therapy to the efficacy of MMFBSA therapy26 week

    the percentage of subjects achieving at least partial remission of LN (PRR) as per the adapted ACR/EULAR Criteria at Week 26