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Merck & Co said it is planning to submit regulatory applications for letermovir in the US and European Union sometime this year, on the back of late-stage data showing its promise in preventing a serious viral infection in patients undergoing a bone marro
Letermovir Prophylaxis Associated with Lower All-Cause Mortality Through Week 24 Post-Transplant. Company Plans to Submit New Drug Applications for Letermovir in U.S. and EU in 2017.