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RECRUITING
NCT07611214
PHASE4

PRESERVE: LUPKYNIS in Combination With Belimumab, Obinutuzumab or Anifrolumab in Patients With Lupus Nephritis

Sponsor: Aurinia Pharmaceuticals Inc.

View on ClinicalTrials.gov

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

DRUG

LUPKYNIS

voclosporin

BIOLOGICAL

belimumab, obinutuzumab or anifrolumab

BENLYSTA (belimumab), GAZYVA (obinutuzumab) or SAPHNELO (anifrolumab)

DRUG

mycophenolic acid analog (MPAA)

CELLCEPT (mycophenolate mofetil \[MMF\]) or MYFORTIC (mycophenolic acid \[MPA\])

DRUG

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