Phase 4 Lupus Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults between 18 and 75 years old
- People who have been diagnosed with lupus nephritis (a form of kidney disease linked to lupus) confirmed by a kidney biopsy, classified as class III, IV, III/V, or IV/V under a standard medical classification system
- People whose urine test shows a protein-to-creatinine ratio of at least 0.5 but less than 5.0 g/g, measured from a first morning urine sample
- People whose kidneys are functioning at a level of at least 45 mL/min/1.73 m² as measured by a standard kidney function test (eGFR)
- People who are already receiving, or who will begin receiving by Day 1 of the trial, one of the following medications: belimumab, anifrolumab, or obinutuzumab (those on obinutuzumab must have already received at least two doses before the screening stage)
- People who are willing to take a medication called a mycophenolic acid analog (MPAA), either by continuing a current prescription or starting it by Day 1
- People who are willing to take corticosteroids (such as prednisone or an equivalent), either by continuing a current prescription or starting it by Day 1
Who may not be able to join:
- People who have received any B-cell targeted therapy (other than belimumab or obinutuzumab) within the past year, unless blood tests show their B-cell count is back within the normal range
- People who have taken cyclophosphamide, or certain immune-suppressing medications called calcineurin inhibitors (such as cyclosporine or tacrolimus, but not voclosporin), within the past 3 months
- People who have taken certain other immune-suppressing medications within roughly the past 30 days or longer (depending on how long the medication stays in the body), including TNF-blocking therapies (such as adalimumab, etanercept, or infliximab), certain anti-inflammatory biologics (such as tocilizumab, ustekinumab, or dupilumab), a T-cell targeting medication called abatacept, intravenous immunoglobulin (IVIg), or JAK inhibitor medications such as upadacitinib (confirm with trial site for the full list)
- People who are pregnant, breastfeeding, or planning to become pregnant during the trial
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 833-606-5975
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
To assess the efficacy of LUPKYNIS in combination with belimumab, obinutuzumab or anifrolumab at inducing rapid renal response: Proportion of patients with complete renal response at 24 weeks
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.