Video content above is prompted by the following questions:
Please provide an overview of the AGAVE-201 trial, including its design, patient population, and key endpoints.
What were the primary and secondary endpoints of the AGAVE-201 trial, and how were they assessed?
How did the trial evaluate the efficacy, safety, and tolerability of different dosing regimens of axatilimab in patients with recurrent or refractory active chronic GVHD?
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