Investor Day 2025
Logotype for Xeris Biopharma Holdings Inc

Xeris Biopharma (XERS) Investor Day 2025 summary

Event summary combining transcript, slides, and related documents.

Logotype for Xeris Biopharma Holdings Inc

Investor Day 2025 summary

8 Jul, 2026

Strategic vision, leadership, and growth trajectory

  • Focused on long-term value creation and accelerated growth through innovation in endocrine and rare disease therapies, leveraging proprietary technologies and operational excellence.

  • Leadership team with deep experience in pharmaceutical development, commercialization, and operational excellence.

  • Revenue guidance raised to $260M–$275M for 2025, targeting $750M by 2030 and multi-billion dollar revenue by 2035, driven by Recorlev and XP-8121.

  • Financial strength enables self-funding of growth initiatives, with at least 85% gross margins and positive adjusted EBITDA, eliminating the need for additional capital.

  • Open to partnerships for value-adding opportunities but not reliant on them for funding or execution.

Recorlev: Market opportunity and commercial strategy

  • Recorlev, a differentiated therapy for Cushing's syndrome, is expected to reach $1B in annual net revenue by 2035, with ongoing investments in commercial expansion, patient support, and data generation.

  • Stepwise investments include sales force expansion, infrastructure enhancements, and real-world evidence generation to strengthen value proposition and payer engagement.

  • Focus on broadening screening and diagnosis of hypercortisolism, targeting both visible and non-visible patient presentations to capture unmet needs and drive market growth.

  • Lifecycle management includes defending IP (patents to 2040), exploring new indications, and combination therapies to ensure brand durability.

  • Recorlev's unique mechanism addresses the root cause of Cushing's syndrome, normalizes cortisol, improves clinical outcomes, and supports individualized therapy.

XP-8121: Innovation in hypothyroidism management

  • XP-8121, a once-weekly subcutaneous levothyroxine, bypasses GI absorption and targets 3M–5M US patients with inconsistent control on oral therapy.

  • Phase III pivotal study to begin in 2026, aiming for approval by 2030, with a 1,000-patient, 54-week trial comparing XP-8121 to oral therapy on TSH normalization.

  • Peak sales projected at $1B–$3B, supported by strong prescriber and patient interest due to unmet needs and dissatisfaction with current therapies.

  • Product leverages proprietary XeriSol technology and established regulatory pathways, with development and launch fully funded by internal cash flow.

  • High patient and physician interest due to improved compliance and predictable pharmacokinetics.

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