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Alnylam Suspends Fitusiran Dosing due to Thrombotic Event

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The following is an edited version of a press release from Alnylam Pharmaceuticals. To read the press in full, click here.


Alnylam recently became aware of a fatal serious adverse event (SAE) that occurred in a patient with hemophilia A who was receiving fitusiran in the Phase 2 OLE study. As a result, the Company has suspended dosing in all ongoing fitusiran studies pending further review of the safety event and development of a risk mitigation strategy.

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