LUPKYNIS + Other Treatments for Lupus Nephritis
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial examines how well LUPKYNIS works with other treatments to quickly improve kidney health in people with lupus nephritis, a kidney condition related to lupus. Participants will take LUPKYNIS alongside one of three other medications: belimumab, obinutuzumab, or anifrolumab, in addition to mycophenolic acid analog and corticosteroids. The study targets individuals diagnosed with lupus nephritis through a biopsy and who have specific protein levels in their urine. As a Phase 4 trial, it involves an FDA-approved treatment and aims to understand how LUPKYNIS can benefit more patients.
Do I need to stop my current medications for the trial?
You may need to stop certain medications before joining the trial. Specifically, you cannot have taken B cell targeted therapies (except for belimumab and obinutuzumab) within the past year, cyclophosphamide or certain calcineurin inhibitors within the past 3 months, or other immunosuppressive therapies within the past 30 days or 5 half-lives, whichever is longer. However, you can continue taking mycophenolic acid analogs and corticosteroids.
What is the safety track record for these treatments?
In previous studies, LUPKYNIS® (voclosporin) was well-tolerated, with no unexpected safety issues reported over three years. However, it increases the risk of serious infections and certain cancers. Most patients, about 86%, experienced some side effects, which were generally expected with this type of medication.
Research shows that belimumab is safe and helps improve kidney health. Reports of serious allergic reactions, such as anaphylaxis, are rare.
Testing has shown that obinutuzumab has a safety profile typical for its class, though some patients may experience serious reactions during the first treatment.
Studies indicate that anifrolumab is generally well-tolerated, but it can weaken the immune system, leading to serious infections in some cases.
The FDA has approved all these treatments for other conditions, suggesting their safety is well understood. However, discussing any concerns with a healthcare provider is important.12345Why are researchers enthusiastic about this study treatment?
Researchers are excited about LUPKYNIS for lupus nephritis because it offers a unique approach compared to traditional treatments like corticosteroids and immunosuppressants. Unlike these standard therapies, LUPKYNIS works by selectively modulating the body's immune response, potentially reducing the risk of long-term damage to the kidneys. Additionally, when combined with other targeted therapies like belimumab, obinutuzumab, or anifrolumab, LUPKYNIS may enhance treatment effectiveness, offering a more comprehensive strategy for managing lupus nephritis. This novel approach could lead to better outcomes and improved quality of life for patients.
What evidence suggests that this trial's treatments could be effective for lupus nephritis?
Research has shown that LUPKYNIS (voclosporin), which participants in this trial may receive, effectively treats lupus nephritis by quickly lowering protein levels in urine, crucial for kidney health. Studies have found that more patients using LUPKYNIS experience improved kidney function. In this trial, LUPKYNIS will be combined with either belimumab, obinutuzumab, or anifrolumab. Belimumab shows promise by reducing the risk of kidney problems and helping prevent flare-ups of lupus nephritis symptoms. Obinutuzumab enhances kidney health by reducing protein in urine and increasing the number of patients with improved kidney function. Anifrolumab may help reduce the risk of long-term organ damage in people with lupus, although its specific effects on kidneys remain less clear. Each treatment offers a unique approach to managing lupus nephritis, with evidence supporting their role in improving kidney health.12567
Are You a Good Fit for This Trial?
This trial is for adults with lupus nephritis, a kidney problem caused by lupus. Participants should be able to take immune-suppressing medicines and not have other serious health issues that could interfere with the study.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Patients receive LUPKYNIS in combination with belimumab, obinutuzumab, or anifrolumab, along with mycophenolic acid analog and corticosteroids
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Anifrolumab
- Belimumab
- LUPKYNIS
- Obinutuzumab
Trial Overview
The study tests LUPKYNIS combined with either belimumab, obinutuzumab, or anifrolumab—alongside standard treatments like mycophenolic acid analogs and corticosteroids—to see which combination helps kidneys recover fastest in people with lupus nephritis.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Patients will also receive concomitant mycophenolic acid analog and corticosteroids.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Aurinia Pharmaceuticals Inc.
Lead Sponsor
Citations
Anifrolumab in lupus nephritis: results from second-year ...
Through Week 52, 41 patients (80%) receiving anifrolumab IR, 32 (71%) receiving anifrolumab BR and 28 (57%) receiving placebo completed study ...
Saphnelo demonstrates higher rates of remission in ...
This was an increase from 19.7% (n=49/251) of patients treated with Saphnelo who achieved remission at the first LTE visit (Week 64) compared ...
3.
astrazeneca.com
astrazeneca.com/content/az-us/media/press-releases/2022/first-patients-dosed-in-iris-phase-iii-trial-evaluating-anifrolumab-in-lupus-nephritis.htmlFirst patients dosed in IRIS Phase III trial evaluating ...
Although the trial's primary endpoint was not met (69% versus 70%, p=0.905), the higher dose tested showed clinically meaningful numeric ...
NCT05138133 | Phase 3 Study of Anifrolumab in Adult ...
The purpose of this study is to evaluate the efficacy and safety of IV antifrolumab in adult patients with Active Proliferative Lupus Nephritis
Phase II randomised trial of type I interferon inhibitor ...
At W52, 24-hour UPCR improved by 69% and 70% for combined anifrolumab and placebo groups, respectively (geometric mean ratio=1.03; 95% CI 0.62 to 1.71; p=0.905) ...
SAPHNELO approved in the US for subcutaneous self- ...
SAPHNELO IV is the first biologic with remission data in SLE from a four-year placebo-controlled Phase III trial (TULIP-LTE) measured with the ...
SAPHNELO® (anifrolumab-fnia) for Systemic Lupus ...
The efficacy of SAPHNELO has not been evaluated in patients with severe active lupus nephritis or severe active central nervous system lupus.
Unbiased Results
We believe in providing patients with all the options.
Your Data Stays Your Data
We only share your information with the clinical trials you're trying to access.
Verified Trials Only
All of our trials are run by licensed doctors, researchers, and healthcare companies.