Stock Taper Total Revenue: $92 million, a 29% increase year-over-year.
Net Product Revenue: $91 million, up 34% year-over-year.
Recorlev Revenue: $56.8 million, representing 81% growth year-over-year.
Gvoke Revenue: Approximately $23 million, a 10% sequential increase.
Keveyis Revenue: Nearly $12 million, reflecting stable performance.
Gross Margin: Approximately 86%, an improvement of nearly 400 basis points year-over-year.
R&D Expenses: $10.7 million, up $2.6 million year-over-year.
SG&A Expenses: $61 million, primarily due to the expanded Recorlev commercial team.
Adjusted EBITDA: $19.3 million, a 50% year-over-year increase.
Convertible Notes: Fully retired, eliminating $3 million in annual interest expense.
Recorlev: Continued strong performance with record patient referrals and prescriber confidence. The company aims to establish Recorlev as the standard of care for endogenous Cushing's syndrome.
Gvoke: After a slow start, Gvoke is showing signs of recovery with expectations for further growth during the back-to-school season.
Keveyis: Received a notice of allowance for a new patent, extending protection through at least 2039, allowing for continued investment in patient outreach.
XP-8121 Pipeline: Significant progress with the program, including two new patents received and plans for Phase III initiation by year-end. A webinar is scheduled for September 9 to discuss the program in detail.
Revenue Guidance: Increased bottom end of full-year 2026 revenue guidance to $385 million - $390 million, reflecting confidence in continued growth.
SG&A Increase: Expected full-year increase of approximately $50 million, up from previous guidance of $45 million, to support commercial expansion.
R&D Spending: Anticipated increase of $25 million for XP-8121, with similar increases expected as the trial ramps up.
Guidance Ceiling: While the lower end of revenue guidance was raised, the upper end remained unchanged at $390 million, indicating potential limitations in growth expectations.
Market Dynamics: The company noted that the market for Recorlev is complex, requiring significant effort for patient diagnosis and treatment, which may slow growth.
Competitive Pressures: The presence of generics in the market for Keveyis could pose risks, although the new patent provides some protection.
Market Growth for Recorlev: Over 60% of patients are new to therapy, indicating a strong capture of new patient starts, but specific market size data was not disclosed.
Phase III Program for XP-8121: The company emphasized that the Phase III trial will not start until all commercial preparations are complete, with timelines expected to be clarified in the upcoming webinar.
Business Development: Xeris is actively seeking growth opportunities that leverage its existing commercial infrastructure, particularly in endocrinology and rare diseases. Overall, Xeris Biopharma reported a strong second quarter with significant revenue growth and strategic advancements, while also addressing challenges related to market dynamics and competitive pressures. The company remains optimistic about its future growth trajectory.
SOURCE: Q2 2026 EARNINGS CALL TRANSCRIPT