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.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
The Pediatric Lupus Nephritis Mycophenolate Mofetil (PLUMM) Study
At a glance
Conditions
Where it's being run
19 sites across 14 statesStudy leadership
- Hermine I Brunner, MD · PRINCIPAL_INVESTIGATOR · Children's Hospital Medical Center, Cincinnati
Who to contact
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What this trial measures
- 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