The Lupus Research Alliance congratulates Aurinia Pharmaceuticals Inc. on acceptance of its NDA filing and priority review designation by the U.S. Food and Drug Administration for its investigational drug voclosporin for lupus nephritis. A serious inflammation of the kidneys, lupus nephritis is one of the most common complications of system
NEW YORK, July 22, 2020 /PRNewswire/ -- Alliance For Lupus Research congratulates Aurinia Pharmaceuticals Inc. on acceptance of its NDA filing and priority review designation by the U.S. Food and Drug Administration for its investigational drug voclosporin for lupus nephritis. A serious inflammation of the kidneys, lupus nephritis is one of the most common complications of systemic lupus erythematosus. Currently, there are treatments approved by the FDA for lupus nephritis. The FDA grants priority review designation to the evaluation of drugs that, if approved, would be significant improvements in the safety or effectiveness of the treatment for serious conditions. Under this designation, the Agency sets a goal to review and act upon the application within six months; in contrast, standard review can take ten months. The company anticipates having a decision from the FDA by early 2021. "If approved by the FDA, voclosporin would be the first treatment approved specifically for this devastating complication that affects up to half of the five million people worldwide with lupus," noted Lupus Research Alliance President and CEO Kenneth M. Farber. "Lupus nephritis can cause irreparable damage to the kidneys that requires dialysis or an organ transplant. A new treatment for lupus nephritis could dramatically change the lives of people with lupus." Key Lupus Nephritis Statistics from the National Institutes of Health:
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