02
Dec

A small Phase I/II study of Prothena’s lead drug produced an encouraging round of initial responses among patients with AL amyloidosis, a rare threat to organs. And now company execs say they’re going straight into a Phase III study of NEOD001 so they can build a case for regulators.

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Source: Prothena gets a positive snapshot of efficacy for rare disease drug, preps for PhIII

    

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