The Pediatric Lupus Nephritis Mycophenolate Mofetil (PLUMM) Study
Study Details
Study Description
Brief Summary
The study is a 1-year 2-part double-blinded placebo controlled 2-arm clinical trial. Treatment arms are (1) MMF dosed as per body-surface area (MMFBSA; 600mg/m2 body surface area per dose about every 12 hours) and (2) pharmacokinetically-guided precision-dosing of MMF (MMFPK; MMF dosed twice daily to achieve an area under the concentration-time curve (AUC0-12h) of MPA >60-70 mg*h/L. The study goal is to determine the safety and efficacy of MMFPK compared to MMFBSA for the treatment of proliferative LN in subjects 8 to <18 years.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
Subjects will be randomized 1:1 to receive blinded treatment with MMFPK or MMFBSA for up to 53 weeks. The primary endpoint, clinical remission of LN, is measured at the end of Part 1 at week 26. Subjects in the MMFBSA arm who have only partial renal response (PRR) at the end of Part 1 will newly receive MMFPK upon entering Part 2 of the study (week 26 - 53). Subjects with complete renal responses (CRR) at the end of Part 1 will continue the same dosing regimen of MMF (MMFBSA or MMFPK) in Part 2 as was given in Part 1 of the study. Subjects in the MMFPK arm with PRR at the end of Part 1 will enter Part 2 and continue in the MMFPK arm.
Subjects who are LN non-responders by the end of Part 1 at week 26 will be considered treatment failures and discontinued from the study intervention. All subjects who are discontinued from the study intervention for reasons of efficacy or safety will receive LN treatment and monitoring as per the treating physician's decision. However, these subjects will be asked to participate in study visits at weeks 26 and 53/End of Study.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: MMFBSA MMF dosed as per body-surface area |
Drug: Mycophenolate Mofetil
MMF dosed 600mg/m2 body surface area per dose about every 12 hours
Other Names:
|
| Experimental: MMFPK MMF dosed as per pharmacokinetically-guided precision-dosing |
Drug: Mycophenolate Mofetil
MMF dosed twice daily to achieve an area under the concentration-time curve (AUC 0-12h) of MPA >=60-70 mg*h/L
Other Names:
|
Outcome Measures
Primary Outcome Measures
- To compare the efficacy of MMFPK therapy to the efficacy of MMFBSA therapy [26 week]
the percentage of subjects achieving at least partial remission of LN (PRR) as per the adapted ACR/EULAR Criteria at Week 26
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Male or female aged 8 to < 18 years;
-
Must meet Classification Criteria for SLE as per the criteria of the American College of Rheumatology (ACR)/ European League Against Rheumatism 1-3 (Appendix 0);
-
Newly diagnosed with proliferative LN as per the International Society of Nephrology/Renal Pathology Society based on kidney biopsy done within 60 days prior to enrollment into the study; Subjects may have been previously diagnosed with other Classes of LN. For study inclusion, the kidney biopsy must be newly interpreted as one of the following classes: Class 3, Class 3/5, Class 4, or Class 4/5.
-
SLEDAI renal domain score > 0;
-
Treatment of LN with twice daily MMF as per the decision of the treating physician. During the screening period the subject will take MMF as prescribed by their treating physician for a minimum of 4 days (or 8 doses).
-
Subject tolerates MMF as per the treating physician's opinion;
-
Able to swallow MMF tablets and capsules;
-
Subjects may be treated with hydroxychloroquine. The allowable dose of hydroxychloroquine cannot exceed 5 mg/kg/day and the medication must have been started at least 1 week prior to Baseline visit;
-
Subjects who are treated with belimumab must be on a stable dose 3 months prior to the Baseline visit;
-
Subjects who are willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures;
-
Evidence of a personally signed and dated Informed Consent document and Assent document (as appropriate) indicating that the subject and a legally acceptable representative/ parent(s)/legal guardian has been informed of all pertinent aspects of the study.
-
Parent or legal guardian must have a smart phone available and able to support the PLUMM smart phone application.
-
Must be able to complete study questionnaires in English or Spanish
Exclusion Criteria:
-
Perceived or stated inability to adhere to the study protocol;
-
Hypersensitivity to MMF or any component of the drug product;
-
Presence of features (from SLE or other chronic disease) that a-priori suggest that the subject benefits from other therapies than that suggested or allowable by the study protocol; These disease features include but are not limited to severe, progressive, or uncontrolled hepatic, hematologic, gastrointestinal, metabolic, endocrine, pulmonary, cardiac or neurologic disease.
-
History of other kidney disease besides LN or prior to the diagnosis of SLE;
-
Need for renal replacement therapy within 2 weeks from Baseline. Subjects can have required short-term renal replacement therapy prior to Baseline, for example due to preceding acute kidney injury.
-
Infections:
-
Untreated latent or active tuberculosis (TB);
-
Chronic infections requiring treatment;
-
A subject known to be infected with Human Immunodeficiency Virus (HIV), Hepatitis B, or Hepatitis C;
-
Any infection requiring hospitalization, parenteral antimicrobial therapy or judged to be opportunistic by the investigator within 4 weeks prior of Baseline visit;
-
Any treated infections within 2 weeks of Baseline visit;
-
History of infected joint prosthesis with prosthesis still in situ;
-
Blood dyscrasias, including:
-
Hemoglobin <8.5 g/dL or Hematocrit <22%;
-
White Blood Cell count <2.6 x 109/L;
-
Neutrophil count <1.2 x 109/L;
-
Platelet count <100 x 109/L;
-
Lymphocyte count <0.5 x 109/L.
-
Estimated glomerular filtration rate [GFR] <40 mL/min/1.73 m2 calculated using the modified Schwartz equation5 (see Appendix 4);
-
Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) >1.5 times the upper limit of normal;
-
Vaccinated or exposed to a live or attenuated vaccine within the 4 weeks prior to Baseline visit;
-
History or current symptoms suggestive of lymphoproliferative disorders (e.g. Epstein Barr Virus [EBV] related lymphoproliferative disorder, lymphoma, leukemia, myeloproliferative disorders, or multiple myeloma);
-
Current malignancy or history of any malignancy with the exception of adequate treated or excised basal cell or squamous cell or cervical cancer in situ;
-
Recent (within 4 weeks prior to Baseline visit) significant trauma or major surgery;
-
Herbal supplements with pharmaceutical properties must be discontinued at least 4 weeks prior to Baseline visit, unless there are sufficient data available regarding the duration of an herbal medication's pharmacokinetic and pharmacodynamic effects to allow a shorter or longer washout to be specified (e.g. 5 half-lives).
-
Oral or intravenous cyclophosphamide must be discontinued 12 weeks prior to Baseline visit
-
Rituximab or other selective B lymphocyte depleting agents: Must be discontinued for 6 months prior to Baseline visit or CD19/20+ counts must be normal by FACS analysis;
-
Use of prohibited prescription medication as listed in Appendix 3 within the specified time frame prior to Baseline visit
-
Participation in other studies involving investigational drug(s) within 4 weeks or 5 half-lives (whichever is longer) prior to Baseline visit and/or during study participation; Exposure to investigational biologics should be discussed with the Sponsor.
-
Pregnant female subjects; breastfeeding female subjects; male subjects with partners currently pregnant; male subjects able to father children and female subjects of childbearing potential who are unwilling or unable to use two highly effective methods of contraception or are abstinent (see Section 4.4.) for the duration of the study;
-
Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the subject inappropriate for entry into this study.
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Children's Hospital Medical Center, Cincinnati
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
- Genentech, Inc.
Investigators
- Principal Investigator: Hermine I Brunner, MD, Children's Hospital Medical Center, Cincinnati
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- ML42264
- 1R01AR079124-01A1