Redeye comments on Faron’s announcement that the phase II BEXMAB trial has met its primary endpoint in treatment-resistant high-risk MDS. We are encouraged to see topline results confirming earlier interim data, with sustained high response rates in this difficult-to-treat population and a continued strong safety profile. These findings not only validate bexmarilimab’s clinical potential but also support Faron’s regulatory and commercial strategy as the company prepares for pivotal phase III development.

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