AstraZeneca Says Rare Disease Drug Shows Improvements in Inherited Bone Disorder Despite Missing Key Trial Goal
AstraZeneca releases Phase 3 HICKORY trial data for efzimfotase alfa in hypophosphatasia (HPP), showing key secondary improvements.
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Why It Matters
AstraZeneca's new rare bone disease drug worked better than expected in some ways. Even though it missed its main trial goal, the company found helpful improvements that doctors will study.
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