PRESERVE: LUPKYNIS in Combination With Belimumab, Obinutuzumab or Anifrolumab in Patients With Lupus Nephritis
Recruiting · NCT07611214 · Interventional (participants receive a specific treatment) · Lead sponsor: Aurinia Pharmaceuticals Inc.
View the official record on ClinicalTrials.gov →Interventions studied
What this trial is about
The goal of this clinical study is to assess the efficacy and safety of LUPKYNIS® in combination with belimumab, obinutuzumab or anifrolumab at inducing rapid renal response in patients with lupus nephritis (LN).
Who can take part
Age range
18 Years to 75 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 4
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Adults 18-75 years old
- Diagnosed with biopsy-proven lupus nephritis (LN) according to the 2003 International Society of Nephrology (ISN) / Renal Pathology Society (RPS) (class III, class IV, class III/V or class IV/V)
- Urine protein-to-creatine ratio (UPCR) ≥0.5 g/g and \<5.0 g/g from a first morning void (FMV) urine sample
- Estimated glomerular filtration rate (eGFR) of ≥45 mL/min/1.73 m2
- Concomitant biologic:
- Patients on the belimumab or anifrolumab treatment regimens are receiving belimumab or anifrolumab (as applicable) prior to Screening or will initiate belimumab or anifrolumab (as applicable) on or before Day 1.
- Patients on the obinutuzumab treatment regimen must have received at least 2 administrations of obinutuzumab prior to Screening.
- Willing to take mycophenolic acid analog (MPAA), either by continuing current MPAA therapy or by initiating it on or before Day 1
- Willing to take corticosteroids, either by continuing current corticosteroids (prednisone \[or equivalent\]) or by initiating on or before Day 1
- Key
Exclusion criteria
- Any B cell targeted therapy except for the concomitant biologics (belimumab and obinutuzumab) within 1 year prior to Screening unless demonstration of B cell count within the normal range
- Cyclophosphamide or any calcineurin inhibitor other than voclosporin (eg, cyclosporine and tacrolimus) within 3 months prior to Screening
- Any other immunosuppressive therapy except for the concomitant drugs (anifrolumab, MPAAs and oral prednisone \[or equivalent\]) and immunosuppressive agents used to treat a patient's underlying systemic lupus erythematosus (SLE), including, but not limited to, the examples below, within 30 days or 5 half-lives, whichever is longer, prior to Screening:
- Anti-tumor necrosis factor (TNF) therapy (eg, adalimumab, etanercept, infliximab)
- Anti-interleukin therapy (eg, risankizumab, secukinumab, ixekizumab, ustekinumab, guselkumab, tocilizumab, dupilumab)
- T cell costimulation modulator (eg, abatacept)
- Intravenous immunoglobulin (IVIg)
- Janus kinase (JAK) inhibitors (eg, upadacitinib)
- Pregnant, breastfeeding or intending to become pregnant during the Study
Where it is running
27 locations listed across 15 US states.
- Purushotham & Akther Kotha MD, Inc. - La Mesa, California, United States
- Valerius Medical Group & Research Center of Greater Long Beach, Inc. - Los Alamitos, California, United States
- Western Nephrology & Metabolic Bone Disease, PC - Arvada, Colorado, United States
- Swati Shah MD Rheumatology, LLC - Jacksonville, Florida, United States
- Vida Clinical Research - Kissimmee, Florida, United States
- Life Clinical Trials - Margate, Florida, United States
- CTR Oakwater - Orlando, Florida, United States
- Parris and Associates Rheumatology - Lawrenceville, Georgia, United States
- Accurate Clinical Research, Inc. - Lake Charles, Louisiana, United States
- Arthritis and Rheumatism Associates - Rockville, Maryland, United States
- Kansas City Physician Partners - Kansas City, Missouri, United States
- University of Nevada Las Vegas - Las Vegas, Nevada, United States
- Sahni Rheumatology & Therapy - West Long Branch, New Jersey, United States
- Buffalo Rheumatology and Medicine, PLLC - Orchard Park, New York, United States
- Arthritis and Osteoporosis Consultants of the Carolinas - Charlotte, North Carolina, United States
- Joint and Muscle Research Institute - Charlotte, North Carolina, United States
- Rheumatic Disease Associates, Ltd. - Willow Grove, Pennsylvania, United States
- Dunes Clinical Research - Dakota Dunes, South Dakota, United States
- West Tennessee Research Institute - Jackson, Tennessee, United States
- Novel Research LLC - Bellaire, Texas, United States
- Liberty Research Center - Dallas, Texas, United States
- Texas Arthritis Center - El Paso, Texas, United States
- Integrative Rheumatology of South Texas - Harlingen, Texas, United States
- Northwest Houston Arthritis Center - Houston, Texas, United States
- Texas Tech University Health Science Center - Lubbock, Texas, United States
- Texas Rheumatology Research Institute, LLC - Plano, Texas, United States
- Nephrology Leaders and Associates, PLLC - Van Vleck, Texas, United States