Oppenheimer 35th Annual Healthcare Life Sciences Conference (Virtual) 2025
Logotype for Xeris Biopharma Holdings Inc

Xeris Biopharma (XERS) Oppenheimer 35th Annual Healthcare Life Sciences Conference (Virtual) 2025 summary

Event summary combining transcript, slides, and related documents.

Logotype for Xeris Biopharma Holdings Inc

Oppenheimer 35th Annual Healthcare Life Sciences Conference (Virtual) 2025 summary

23 Dec, 2025

Portfolio overview and product performance

  • Three main products: Gvoke (diabetes rescue), Recorlev (Cushing's/hypercortisolism), and Keveyis (PPP), with Gvoke and Recorlev as primary growth drivers.

  • Gvoke leverages XeriSol technology for a ready-to-use glucagon, replacing older, less user-friendly kits.

  • Recorlev targets cortisol synthesis, gaining adoption among endocrinologists for its direct mechanism and is driving significant revenue growth.

  • Keveyis, despite generic competition, maintains strong brand loyalty due to support services and patient/physician preference.

  • Recent partnership with ADA aims to increase awareness and compliance for Gvoke among the 15 million at-risk patients.

Commercial strategy and market dynamics

  • Expanded sales force by 50% in Q3, accelerating patient referrals and starts, especially for Recorlev.

  • Focus on shifting standard of care to standard of practice for Gvoke, emphasizing clinician and patient education.

  • Entered a development agreement with Beta Bionics for pump-compatible glucagon, with formulation delivered and regulatory progress ongoing.

  • U.S.-centric commercial focus, with international expansion pursued through partnerships; recently ended direct European Gvoke distribution.

  • Ongoing confidential collaborations using XeriSol and XeriJect technologies, with public disclosure tied to material revenue impact.

Pipeline and innovation

  • XP-8121, a once-weekly subcutaneous levothyroxine, addresses unmet needs for patients not normalized on oral therapy, targeting 20%+ of current users.

  • XP-8121 leverages proprietary technology, with supportive PK data and ongoing FDA discussions; phase 3 trial planning underway with mid-year update expected.

  • Physician feedback highlights significant interest due to challenges in managing oral therapy patients.

  • Pipeline development is balanced with financial discipline and top-line growth.

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