Phase 4 Lupus Trial, Recruiting NCT07611214 Sponsor: Aurinia Pharmaceuticals Inc. Condition: Lupus
Back to Lupus

Phase 4 Lupus Trial, Recruiting

NCT07611214
Recruiting Phase 4

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 4 trials study a drug that has already been approved, monitoring long-term safety and effectiveness in real-world use.

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

Status
Recruiting
Phase
Phase 4
Sponsor
Aurinia Pharmaceuticals Inc.
Registry
ClinicalTrials.gov
Start date
22 April 2026
Est. completion
2 March 2029

Where this trial is recruiting

🇺🇸 United States

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?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov