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December 8, 2025Blood

Safety and feasibility of 0.6 mg/kg every 4 weeks dosing of axatilimab in patients treated in the AGAVE-201 study

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Authors

MSMaria Sola Soto

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Overview

Observational analysis showing safety and treatment discontinuations in patients receiving axatilimab for cGVHD, suggesting feasibility of a new dosing strategy.

Key Points

  • Axatilimab, a monoclonal antibody, demonstrates safety and efficacy in chronic graft-versus-host disease (cGVHD).
  • Seventy-three percent of patients achieved a response, with a reported overall response rate of 94.7% after switching doses.
  • This assessment involved patients transitioning from a 0.3 mg/kg Q2W to 0.6 mg/kg Q4W dosing schedule over several cycles.
  • Findings call for careful consideration of dosing schedules for improved safety and continued treatment in cGVHD patients.

Cite This Study

Maria Sola Soto (2025) studied this question.

synapsesocial.com/papers/69362f604fa91c937236dd44https://doi.org/10.1182/blood-2025-272
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