EligibleTrials

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

Recruiting · NCT07611214 · Interventional (participants receive a specific treatment) · Lead sponsor: Aurinia Pharmaceuticals Inc.

View the official record on ClinicalTrials.gov →
Lupus

Interventions studied

LUPKYNISbelimumab, obinutuzumab or anifrolumabcorticosteroidmycophenolic acid analog (MPAA)

What this trial is about

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).

Who can take part

Age range
18 Years to 75 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 4
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

27 locations listed across 15 US states.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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