Arrowhead, Takeda liver drug headed to PhIII despite placebo response's dent on stock
Arrowhead Pharmaceuticals reported Monday that its Takeda-partnered program reduced liver scarring and mutant protein levels in patients with alpha-1 antitrypsin deficiency, a rare liver disease. However, a better-than-expected placebo performance sent shares of Arrowhead $ARWR down more than 20%.
The Phase II SEQUOIA study showed the pair’s RNAi drug candidate fazirsiran reduced markers of AATD, a condition in which the body does not produce enough AAT, a protein made in the liver to protect the lungs.
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