Aurinia Pharmaceuticals Inc Announces Positive Topline Results From the AURORA 2 Continuation Study - Corporate Call Transcript
Greetings, and welcome to the Aurinia Pharmaceuticals Conference Call. (Operator Instructions). As a reminder, this conference is being recorded. I would now like to turn the conference over to Peter Greenleaf, Aurinia's President and CEO. Thank you. You may begin.
Well, thank you, and I want to thank everyone for taking the time during this busy time of the year to join us. Today, we're here to announce the top line results from the conclusion of the AURORA 2 study. To remind you, AURORA 2 is a Phase III continuation study designed to assess the long-term safety and tolerability of voclosporin when added to MMF and low-dose corticosteroids for an additional 24 months following a 52-week treatment period in the original AURORA 1 trial. While there have been interim cuts of the data presented at this year's EULAR and ACR meetings, we now have key data from the completion of the study and are actually quite pleased with the results.
Today, we issued a press release with
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