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PRESERVE: LUPKYNIS in Combination With Belimumab, Obinutuzumab or Anifrolumab in Patients With Lupus Nephritis
Sponsor: Aurinia Pharmaceuticals Inc.
Summary
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).
Official title: PRESERVE: A Multi-Center Phase 4 Study of the Efficacy and Safety of LUPKYNIS in Combination With Belimumab, Obinutuzumab or Anifrolumab at Inducing Rapid Renal Response in Patients With Lupus Nephritis
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
150
Start Date
2026-04-22
Completion Date
2029-03-02
Last Updated
2026-05-28
Healthy Volunteers
No
Conditions
Interventions
LUPKYNIS
voclosporin
belimumab, obinutuzumab or anifrolumab
BENLYSTA (belimumab), GAZYVA (obinutuzumab) or SAPHNELO (anifrolumab)
mycophenolic acid analog (MPAA)
CELLCEPT (mycophenolate mofetil \[MMF\]) or MYFORTIC (mycophenolic acid \[MPA\])
corticosteroid
prednisone (or equivalent)
Locations (10)
Valerius Medical Group & Research Center of Greater Long Beach, Inc.
Los Alamitos, California, United States
Swati Shah MD Rheumatology, LLC
Jacksonville, Florida, United States
CTR Oakwater
Orlando, Florida, United States
Accurate Clinical Research, Inc.
Lake Charles, Louisiana, United States
Arthritis and Osteoporosis Consultants of the Carolinas
Charlotte, North Carolina, United States
Joint and Muscle Research Institute
Charlotte, North Carolina, United States
West Tennessee Research Institute
Jackson, Tennessee, United States
Liberty Research Center
Dallas, Texas, United States
Texas Rheumatology Research Institute, LLC
Plano, Texas, United States
Nephrology Leaders and Associates, PLLC
Van Vleck, Texas, United States