TD Cowen 46th Annual Health Care Conference
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Geron (GERN) TD Cowen 46th Annual Health Care Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Geron Corporation

TD Cowen 46th Annual Health Care Conference summary

2 Mar, 2026

Commercial performance and growth outlook

  • Achieved $184 million in first full year of RYTELO sales, with 2025 revenue guidance of $220–$240 million, reflecting strong anticipated growth.

  • Strategic focus on execution, particularly targeting second-line, low-risk MDS patients, with 80% of business in the community setting.

  • Internal refinements include streamlined organization, targeted messaging, and increased investment in digital and non-personal promotion.

  • Market trends, such as increased frontline use of luspatercept and updated NCCN guidelines, support RYTELO’s positioning as a preferred second-line agent.

  • Key performance indicators include demand growth (9% last quarter), new account orders, and increasing share of first/second-line use (currently 30%).

Market strategy and physician engagement

  • Emphasis on educating community physicians, who manage 80% of patients, through simplified messaging and targeted outreach.

  • Academic centers are engaged with deeper scientific discussions and investigator-sponsored trials (ISTs), with over 10 ISTs approved.

  • ASH data highlights that cytopenia is an on-target, predictable effect, serving as a clinical biomarker for robust response.

  • Real-world evidence and ISTs are expanding understanding of RYTELO’s efficacy across different patient populations and indications.

  • Increased funding for ISTs aims to explore broader applications, including potential use in solid tumors.

International expansion and future catalysts

  • EMA approval secured for RYTELO, with ongoing country-specific funding and pricing strategies in Europe.

  • Ex-U.S. markets seen as significant, with reference to luspatercept’s $500 million ex-U.S. sales.

  • Engaging potential partners and optimizing pricing to reflect innovation and long-term investment.

  • Phase III myelofibrosis (MF) trial interim analysis expected in H2 2025, with full analysis projected for H2 2028.

  • Phase II data showed nearly tripled survival, supporting confidence in the ongoing phase III design.

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