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Biotechnology: Pharmaceutical Preparations
Clinical TrialMay 12, 2026, 09:33 AM

Geron RYTELO Real-World Study Shows 37.5% RBC-TI in LR-MDS Patients

AI Summary

Geron Corporation announced positive real-world evidence for RYTELO (imetelstat) in lower-risk myelodysplastic syndromes (LR-MDS), with data to be presented at the European Hematology Association (EHA) 2026 Congress. The investigator-sponsored study at Moffitt Cancer Center demonstrated safety and efficacy consistent with the Phase 3 IMerge trial in a broader patient population. The study reported a 37.5% red blood cell transfusion independence rate lasting at least eight weeks in heavily pretreated LR-MDS patients. Geron will also present additional data on its myelofibrosis and AML clinical programs at EHA 2026 and ASCO 2026.

Key Highlights

  • Real-world study of RYTELO in LR-MDS showed 37.5% red blood cell transfusion independence (>8 weeks).
  • Study included 40 heavily transfusion-dependent LR-MDS patients with extensive prior therapies.
  • Safety and efficacy were generally consistent with findings from the Phase 3 IMerge trial.
  • Cytopenias were reported as the most common Grade 3/4 adverse event.
  • Exploratory analyses suggested improved responses when RYTELO was used within the first three lines of therapy.
  • Geron will have additional presentations at EHA 2026 and ASCO 2026 on myelofibrosis and AML programs.