Jefferies Global Healthcare Conference 2026
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Camurus (CAMX) Jefferies Global Healthcare Conference 2026 summary

Event summary combining transcript, slides, and related documents.

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Jefferies Global Healthcare Conference 2026 summary

3 Jun, 2026

Business overview and financial performance

  • Profitable commercial operations in opioid use disorder fund a robust late-stage pipeline in endocrinology, oncology, and CNS indications.

  • Achieved 17% revenue growth and record profitability in 2025 despite slower-than-expected growth due to market funding issues.

  • Distribution model changes in the U.K. impacted early 2026 revenues, but normalization and strong growth are expected in the second half of the year.

  • U.K. funding has shifted to a three-year framework, supporting growth plans for 2026.

  • Net cash position around $400 million, with firepower up to $1 billion for strategic acquisitions.

Product portfolio and market opportunities

  • Buvidal targets 100,000 patients in treatment by end of 2027, with 73,000 reached as of 1Q; large European markets like the U.K., Germany, and France offer the most growth potential.

  • U.S. BRIXADI, commercialized by a partner, is seeing strong uptake; first milestone payment expected in the second half of 2026.

  • CAM2029 for GEP-NET aims for improved efficacy and convenience, with a market potential of at least $2 billion; phase III readout expected in the second half of 2026.

  • Oczyesa (Oclaiz) for acromegaly is approved in Germany, with further European launches planned; FDA decision in the U.S. expected imminently.

  • CAM2029 also advancing in polycystic liver disease, with phase III prioritization pending further data.

R&D pipeline and partnerships

  • Obesity program CAM2056 showed strong efficacy and tolerability; phase IIb to start in the second half of 2026, with preparations for phase III underway.

  • Strategic partnership with Eli Lilly expanded to include dual GLP-1, triple-G, and amylin programs, broadening the collaboration's scope.

  • Typical development timelines for established compounds are around 18 months from program initiation to regulatory submission.

  • Milestone payments in partnerships are generally tied to clinical and regulatory achievements.

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