The US Food and Drug Administration yesterday approved Prevymis (letermovir) tablets and injection, the first drug indicated to help prevent CMV (cytomegalovirus) infection and disease in adults who have been exposed to CMV and have received an allogeneic hematopoietic stem cell (bone marrow) transplant (HSCT).
The news pushed the shares of the drug’s maker, Merck & Co (NYSE: MRK), up 1.78% to $56.58 by close of trading yesterday.
Merck purchased worldwide rights to develop and commercialize letermovir from AiCuris GmbH in 2012 for around $570 million. The drug is also under review in Europe, where it has been granted orphan designation.
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