LUPKYNIS with Belimumab, Obinutuzumab, or Anifrolumab for Lupus Nephritis
PRESERVE: LUPKYNIS in Combination With Belimumab, Obinutuzumab or Anifrolumab in Patients With Lupus Nephritis
- Age
- 18 – 75
- Sex
- Any
- Trial phase
- Phase 4
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 150 (estimated)
- Sponsor
- Aurinia Pharmaceuticals Inc. · Industry
This trial is looking for adults with lupus nephritis who want to test a new combination treatment. Participants will need to take some specific medications and be within a certain age range.
You may be able to join if
- I am between 18 and 75 years old.
- I have been diagnosed with lupus nephritis.
- I have a urine protein-to-creatine ratio of at least 0.5.
- I have a kidney function score (eGFR) of at least 45.
- I am currently taking or will start taking mycophenolic acid.
- I am currently taking or will start taking corticosteroids.
- I have received at least 2 doses of obinutuzumab if on that treatment.
You may not be able to join if
- I have received any B cell targeted therapy in the last year.
- I have used cyclophosphamide or certain other medications in the last 3 months.
- I have taken any other immunosuppressive therapy in the last 30 days.
- I am pregnant, breastfeeding, or plan to become pregnant during the study.
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your EligibilityThe 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).
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