US Priority Review for Merck and Bayer's vericiguat

17 July 2020
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The New Drug Application (NDA) for heart med hopeful vericiguat has been accepted for Priority Review by the US Food and Drug Administration.

New Jersey, USA-based Merck & Co (NYSE: MRK) has the American rights to the soluble guanylate cyclase (sGC) stimulator, after entering into a collaboration with German drugmaker Bayer (BAYN: DE).

The firms are developing the candidate to reduce the risk of cardiovascular (CV) death and heart failure hospitalization for people with CV problems.

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