
Phase 3 Data Provide Evidence of Voclosporin as Long-Term Treatment for Lupus Nephritis
A significantly higher number of patients receiving voclosporin achieved good renal outcome when compared with placebo.
According to phase 3 data presented at the
Samir V. Parikh, MD, The Ohio State University Wexner Medical Center, and investigators assessed voclosporin’s safety and efficacy for the treatment of lupus nephritis in the AURORA 1 and AURORA 2 trials. They also evaluated renal outcome over the cumulative 3 year study period.
In AURORA 1, voclosporin was combined with mycophenolate mofetil (MMF) and low-dose steroids and given to patients with lupus nephritis. After a year of treatment, they observed significant reductions in proteinuria in patients on the treatment regimen.
For the next 2 years, this investigation continued as AURORA 2 and patients on the intervention were compared with a placebo group.
All participating patients received MMF and low-dose steroids and depending on which group they were randomized to, also received voclosporin or placebo. Both studies assessed the same outcomes: adverse events (AEs), eGFR, urine protein-creatinine ratio (UPCR), good renal outcome, and renal flare.
Patients who achieved an adequate response (i.e. sustained reduction in UPCR to ≤0.7 mg/mg) and didn’t experience renal flare (i.e. an increase to UPCR >1 mg/mg from a post-response UPCR of <0.2 mg/mg or an increase to UPCR >2 mg/mg from a post-response UPCR of 0.2 to 1.0 mg/mg) were considered to have a good renal outcome.
Not only were the reductions in UPCR maintained throughout the final 2 years, but 66.4% of patients in the intervention group achieved a good renal outcome compared with 54% in the placebo group. Therefore, the effect of voclosporin was clinically significant.
Renal flare with adequate response occurred in 24 of 101 (23.8%) patients taking voclosporin and 19 of 73 (26%) patients in the control group. Investigators noted that 69.8% of all patients with renal flares completed study treatment.
The overall rates of serious adverse events were similar, with 26.7% of those taking voclosporin, and 28% of those taking placebo experiencing at least one. No deaths were reported in the intervention group and 4 deaths were reported in the control group (pulmonary embolism, n=1; coronavirus infection, n=3). The mean eGFR was stable and within normal range for the duration of the study.
“Voclosporin was well-tolerated over 3 years of treatment,” investigators concluded. “The significant reductions in proteinuria initially achieved in AURORA 1 were maintained throughout AURORA 2 and more patients in the voclosporin arm achieved a good renal outcome. These data provide evidence of a long-term treatment benefit of voclosporin in patients with lupus nephritis.”




