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- Merck & Co Inc MRK highlighted findings from a Phase 3 trial of Prevymis (letermovir) compared to valganciclovir for cytomegalovirus (CMV) prophylaxis in high-risk kidney transplant recipients.
- At 52 weeks following the kidney transplant, Prevymis was effective and non-inferior to valganciclovir for preventing CMV disease (10.4% vs. 11.8%).
- Also Read: Centre Piece Of Merck's $11.5B Acceleron Buyout Aces Late-Stage Cardiovascular Trial.
- In a pre-specified safety analysis, Prevymis-treated participants had significantly less myelotoxicity, as measured by rates of leukopenia or neutropenia, compared to valganciclovir-treated participants (26.0% vs. 64.0%).
- The FDA approved Prevymis in 2017 for prophylaxis of CMV infection and disease in adult CMV-seropositive recipients [R+] of an allogeneic hematopoietic stem cell transplant (HSCT).
- Merck is planning to present these data at a scientific congress and will submit a supplemental marketing application with these data to the FDA by the end of this year.
- Price Action: MRK shares closed higher by 2.94% at $95.67 on Friday.
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