Jefferies 2024 Global Healthcare Conference
Logotype for Aurinia Pharmaceuticals Inc

Aurinia Pharmaceuticals (AUPH) Jefferies 2024 Global Healthcare Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Aurinia Pharmaceuticals Inc

Jefferies 2024 Global Healthcare Conference summary

31 Jan, 2026

Commercial performance and financial outlook

  • LUPKYNIS generated nearly $176 million in revenue last year, with 2024 guidance set at $200–$220 million.

  • First quarter results are on track with projections, and the company expects to be cash flow positive in Q2, with $50–$60 million in operating free cash flow projected over the next 12 months.

  • $320 million in cash is held with no debt, and $560 million in net operating losses can offset future revenue.

  • Otsuka partnership has provided $100 million in non-dilutive capital, with a $10 million milestone expected if Japanese approval is secured by year-end.

  • Japan is seen as a lucrative market, and global expansion efforts are ongoing.

Market development and patient engagement

  • Lupus nephritis remains underdiagnosed and undertreated, with less than 50% of lupus patients receiving proper urine screening.

  • Improved diagnosis and adherence to guidelines could double the market size over the next several years.

  • The company is investing in physician and patient education, with campaigns to boost disease awareness and treatment adherence.

  • Patient support includes direct drug shipment, nurse case managers, and high-touch follow-up to ensure persistence.

  • Persistency at 12 and 18 months has reached an all-time high of 56%, with ongoing efforts to standardize restarts for patients who discontinue therapy.

Product differentiation and clinical data

  • LUPKYNIS is the only FDA-approved drug meeting 3- and 6-month proteinuria reduction targets per guidelines.

  • Demonstrates rapid and sustained proteinuria reduction, with a favorable safety profile and no observed kidney harm over three years.

  • The drug is a next-generation calcineurin inhibitor with dual mechanisms, supported by robust clinical and real-world data.

  • Patents extend to 2037, with composition of matter protection until July 2028.

  • Ongoing studies include a real-world registry, pediatric trials, and additional safety assessments.

Partial view of Summaries dataset, powered by Quartr API
AI can get things wrong. Verify important information.
All investor relations material. One API.
Learn more